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Swiss Rolls Recalled Over Salmonella Concerns

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A popular snack treat is being recalled nationwide over potential salmonella concerns.

Swiss Rolls, sold under a variety of brand names including H-E-B and Great Value, are being voluntarily recalled by the manufacturer over the possible presence of salmonella in one of the treat’s ingredients.

Mrs. Freshley’s, Food Lion, H-E-B, Baker’s Treat, Market Square, and Great Value brands are all impacted by the recall nationally, and several southern states are impacted under the Captain John Derst’s Hold Fashioned Bread brand name.

Salmonella can cause serious, or even fatal, infections in young children and the elderly. No human cases have yet been reported in connection with the recall.

For a full list of brand names, UPC label numbers, and Best By Dates, you can visit the Flowers Foods website, or use this list: 

Mrs. Freshleys -4 count/7.2 ounces 
UPC: 072250011907 
Best By Dates: Through 10/19/18 

Mrs. Freshley's - 6 count/12 ounces 
UPC: 072250903233 
Best By Dates:Through 10/14/18

Food Lion - 6 count/13 ounces
UPC: 035826092779
Best By Dates:10/16/18

H-E-B: 6 count/12 ounces 
UPC: 041220296483
Best By Dates:09/19/18

Baker's Treat:6 count/13 ounces 
UPC: 041498188382
Best By Dates:9/21/18 through 9/28/18

Market Square:6 count/12 ounces 
UPC: 087381760556
Best By Dates: 309 8194 B

Great Value: 6 count/13 ounces 
UPC: 078742147550
Best By Dates: 9/17/18 through 9/25/18

Captain John Derst's Old Fashioned Bread
UPC: 071316001180
Best By Dates: 7/16/18 through 7/28/18



Photo Credit: Walmart

Utz Recalls Bags of Carolina Style Barbeque Chips Over Soy Allergen

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Snack food company Utz has recalled select bags of potato chips because of an undeclared soy allergen.

Utz Quality Foods has issued a voluntarily recall on select 2.875 oz. and 7.5 oz bags of Utz Carolina Style Barbeque Potato Chips after learning some packages were mislabeled. The recall affects products distributed in 30 states including Connecticut, D.C., Delaware, Florida, Illinois, Maine, Maryland, Massachusetts, New Hampshire, New Jersey, New York, Pennsylvania, Rhode Island, Texas, Vermont and Virginia, as well as D.C.

No illnesses have been reported, according to the Food and Drug Administration website, but people who have an allergy or severe sensitivity to soy run the risk of a serious or life-threatening allergic reaction if they consume the chips.

Utz urged customers not to eat the chips and either throw them out or return them to the store for a full refund. The company suggested retailers check their shelves and confirm the products are not available for purchase.

The affected 2.875 oz. bags include a UPC code of 0-41780-00153-5 and an expiration date between Oct. 6 and Oct. 20. The affected 7.5 oz. bags include a UPC code of 0-41780-00049-1 and expiration dates between Aug. 18 and Oct. 27.

For more information, email customerservice@utzsnacks.com or call 1-800-367-7629, Monday through Friday, 8:30 a.m. to 5 p.m. ET.



Photo Credit: FDA

40 Hospitalized in Salmonella Outbreak Linked to Raw Turkey

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Ninety people in 26 states have been infected with salmonella in the midst of an outbreak that has been connected to raw turkey products, the Centers for Disease Control and Prevention said Thursday.

There haven’t been any reported deaths, but 40 people have been hospitalized.

Salmonella cases have been reported in Alaska, California, Colorado, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Michigan, Minnesota, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia and Wisconsin, the CDC said in a news release.

While the outbreak hasn’t been linked to a single supplier, the salmonella strain has been found in samples of raw turkey products including pet food and live turkeys, the CDC said.

The agency hasn’t instructed retailers to stop selling raw turkey products and hasn’t told consumers to stop eating properly cooked turkey products.

To avoid being infected with salmonella, the CDC recommends frequently washing your hands, cooking raw turkey thoroughly and avoiding raw diets for pets.

“Always handle raw turkey carefully and cook it thoroughly to prevent food poisoning,” the CDC said in the release. “This outbreak is a reminder that raw turkey products can have germs that spread around food preparation areas and can make you sick.”



Photo Credit: Kevin C. Cox/Getty Images, File

Ritz Crackers, Ritz Bits Recalled Over Salmonella Concerns

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More than a dozen Ritz cracker sandwiches and Ritz Bits products have been recalled due to a possible salmonella contamination, Mondelez Global LLC said.

The New Jersey-based company has recalled sixteen products — including Ritz Cheese Cracker Sandwiches and Ritz Bits Cheese — in the U.S., Puerto Rico and the U.S. Virgin Islands because the whey powder they’re made with could contain salmonella, it said.

Mondelez hasn’t received any reports of people falling ill after eating these products yet, but consumers who have purchased them should throw them out, the company noted.

A full list of the products included in the recall can be found on Mondelez’ website.

“Salmonella is a microorganism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems,” Mondelez said in a release.

Symptoms can include fever, diarrhea, nausea, vomiting and stomach pain, the company said.



Photo Credit: Joe Raedle/Getty Images, File

Pepperidge Farm Recalls 4 Varieties of Goldfish Crackers

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Pepperidge Farm says it has been notified by one of its ingredient suppliers that whey powder in a seasoning that is applied to four varieties of crackers has been the subject of a recall by the whey powder manufacturer due to the potential presence of salmonella.

Pepperidge Farm initiated an investigation and, out of an abundance of caution, is voluntarily recalling four varieties of Goldfish crackers. The products were distributed throughout the United States. 

No illnesses have been reported. No other Pepperidge Farm products in the U.S. are subject to this recall.

The following four varieties with the indicated codes are subject to this recall:

  • Flavor Blasted® Xtra Cheddar
  • Flavor Blasted® Sour Cream & Onion
  • Goldfish® Baked with Whole Grain Xtra Cheddar
  • Goldfish® Mix Xtra Cheddar + Pretzel

Different packaging options are included in this recall. Consumers are encouraged to read this chart.

Consumers who have purchased these products should not eat them. Recalled products should be discarded or may be returned to the place of purchase for a full refund. Consumers with questions may visit www.pepperidgefarm.com/GoldfishUpdate or call Customer Service at 800-679-1791, 24 hours a day, for more information.



Photo Credit: Pepperidge Farm

Taco Bell Salsa Con Queso Recalled Over Botulism Risk

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The Kraft Heinz Company is recalling about 59,000 jars of its Taco Bell Salsa Con Queso Mild Cheese Dip that could potentially lead to botulism if eaten.

Kraft is voluntarily recalling 15-ounce glass jars with "best when used by" dates of Dec. 27, 2018, and Jan. 23, 2019. The affected items are showing signs of product separation, which can allow for the growth of the bacteria that causes botulism, the company said on its website.

Botulism is rare but can be fatal, according to the Centers for Disease Control and Prevention. The illness can cause difficulty breathing and muscle paralysis. Symptoms include blurred or double vision, drooping eyelids, slurred speech, difficulty swallowing, a thick-feeling tongue, dry mouth and muscle weakness.

Kraft said there have been no complaints or reports of illness related to the products. The company said it is working with the Food and Drug Administration.

The affected items were produced and distributed by Kraft in the U.S. The company urged customers not to eat the dip and return it to the store for an exchange or refund.



Photo Credit: Kraft Heinz Company

Pepperidge Farm Recalls 4 Varieties of Goldfish Crackers

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Pepperidge Farm says it has been notified by one of its ingredient suppliers that whey powder in a seasoning that is applied to four varieties of crackers has been the subject of a recall by the whey powder manufacturer due to the potential presence of salmonella.

Pepperidge Farm initiated an investigation and, out of an abundance of caution, is voluntarily recalling four varieties of Goldfish crackers. The products were distributed throughout the United States. 

No illnesses have been reported. No other Pepperidge Farm products in the U.S. are subject to this recall.

The following four varieties with the indicated codes are subject to this recall:

  • Flavor Blasted® Xtra Cheddar
  • Flavor Blasted® Sour Cream & Onion
  • Goldfish® Baked with Whole Grain Xtra Cheddar
  • Goldfish® Mix Xtra Cheddar + Pretzel

Different packaging options are included in this recall. Consumers are encouraged to read this chart.

Consumers who have purchased these products should not eat them. Recalled products should be discarded or may be returned to the place of purchase for a full refund. Consumers with questions may visit www.pepperidgefarm.com/GoldfishUpdate or call Customer Service at 800-679-1791, 24 hours a day, for more information.



Photo Credit: Pepperidge Farm

Why the Food Recalls Might Not Stop With Goldfish and Ritz

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Bill Marler arrived at his Seattle home one night this week and began searching through the cupboard for something to eat. Toward the back, the food poisoning attorney spotted a bag of Goldfish, then remembered news reports about a new recall. Sure enough, he owned one of the more than 3 million packages that had been recalled on Monday. 

The back-to-back recalls of household staples Goldfish and Ritz crackers, along with earlier recalls of the Kellogg's cereal Honey Smacks and other cases, have prompted social media users to question which snacks are safe to eat. The short answer: we don't know yet, though no one has fallen ill from consuming recently recalled snack products linked to one supplier of whey protein.

Pepperidge Farm issued its voluntary recall for four types of its Goldfish crackers after the whey powder manufacturer Associated Milk Producers Inc. (AMPI) announced a recall of its own due to the “possible presence” of salmonella. Another company, Mondelez, recalled several of its Ritz cracker products over the weekend for the same reason.

Last week, Flowers Foods recalled its Swiss Rolls sold under various brand names. The company mentioned the whey powder ingredient in a news release. A Hungry Man frozen dinner also used AMPI's recalled powder. 

AMPI spokeswoman Sarah Schmidt noted that "all products shipped into the marketplace tested negative for Salmonella as part of AMPI’s routine testing program.”

But because "additional product tested positive for Salmonella under AMPI’s routine test and hold procedures," the recall was a precautionary move. 

"At AMPI, we are dedicated to producing dairy products that meet the highest quality and safety standards," Schmidt said. "We will continue to work cooperatively with the FDA." 

In a high-profile recall not linked to AMPI, Kellogg's flagged Honey Smacks last month due to the possible presence of salmonella. Seventy-three people became ill after eating the cereal, according to the Centers for Disease Control and Prevention. Whey powder isn't an ingredient in Honey Smacks, Kellogg's said in an email to NBC. 

Marler, who represents some of the people who fell ill from salmonella after consuming Honey Smacks, said companies that alert customers before anyone gets sick have adopted the best approach to managing the issue.

With Ritz, Goldfish, Swiss Rolls and Hungry Man — products the FDA has linked to AMPI — there haven’t been any reported illnesses. Other manufacturers who use AMPI's whey powder might begin issuing recalls in the coming days, Marler predicted, based on how past recalls have played out. 

"I would expect it to be potentially dozens of products," Marler said. "This kind of recall is the system working properly. It's common and actually a good thing."

Here's how the system operates: ingredient and product testing is not regulated or required by the government. Companies often test their products according to their own food safety plans, said Martin Bucknavage, a senior food safety associate at Penn State’s college of agricultural sciences.

When an ingredient supplier identifies possible contamination, it contacts the manufacturers it works with. The supplier also files a report with the FDA explaining the recall using the agency's reportable food registry portal.  

In AMPI's case, the powder they provide for dairy and baked products is also a common ingredient used to coat cereals and other snacks, said Randy Worobo, a professor in Cornell’s department of food science. 

AMPI declined to release its complete list of whey powder customers,  confirming only that four manufacturers it works with have issued voluntary recalls as of Wednesday. It said it doesn't release proprietary customer lists.

An FDA spokesman said the agency had the list but wouldn't provide it. NBC has filed a Freedom of Information Act request to determine which companies receive whey powder from AMPI. 

Salmonella is a bacteria that causes 1.2 million illnesses and 450 deaths in the U.S. each year, according to the CDC. Food is the cause of 1 million of those illnesses and 380 deaths. 

In 2007 and 2008, Peanut Corporation of America discovered salmonella contamination in its ingredients that were used in other manufacturers’ products but didn’t immediately issue a recall, according to The New York Times. Nine people were killed and more than 700 were reported ill as a result.

Companies that issue voluntary recalls before anyone gets sick will likely be viewed by customers in a positive light, said Tom Meyvis, an NYU marketing professor who studies consumer behavior.

“There’s an advantage to [the recall being connected] to one supplier,” Meyvis said.

Marler, the food poisoning attorney in Seattle, said that between recalls for romaine lettuce and Del Monte vegetables and illnesses linked to McDonald’s salads, the number of food-related ailments this year is alarming.

The FDA disputes that characterization. Commissioner Scott Gottlieb said in a statement that there haven't been an increase in the number or scope of recalls.

"Our tools for detecting them are much better, and our policies for how and when we alert the public lean in the direction of more and earlier communication," Gottlieb said. 

The FDA recommends that people discard or return recalled products to the stores where they're purchased. 



Photo Credit: Pepperidge Farm/Getty Images/AMPI

Federal Health Alert on Wraps, Salads Sold at Trader Joe's

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The United States Department of Agriculture issued a nationwide public health alert for more than two dozen beef, pork and poultry salad and wrap products distributed by Caito Foods LLC, three varieties of which are sold at Trader Joe's, due to concerns about contamination with Cyclospora. The parasite causes intestinal illness.

Caito Foods was notified from their lettuce supplier, Fresh Express, that the chopped romaine used in some of the salads was being recalled, the USDA said.

Trader Joe's identified its three products affected by the recall as Trader Joe's Tarragon Chicken Salad Wrap, Trader Giotto’s Caesar Salad with Chicken and Trader Ming’s Chinese Inspired Salad with Chicken with "Best By" dates of July 21, 2018, to July 23, 2018. The products were sold in stores spanning 11 states: Iowa, Illinois, Indiana, Kansas, Kentucky, Michigan, Minnesota, Missouri, Nebraska, Ohio and Wisconsin. 

Products that were distributed by Gordon Food Service or sold at Kroger and Walgreens were also listed in the recall notice.

A Gordon Food Service representative said that its product — a roast beef wrap, chicken Caesar salad and Santa Fe chicken salad — was sent to a customer in Ohio, who has been notified about the recall. 

Walgreens' affected product — an Asian chicken salad, chicken Caesar and chef salad with ham and turkey — was available "in a limited number of our stores in Illinois only," a spokesperson said. "Upon learning of the recall, we notified these stores to immediately pull and dispose of any product on store shelves."

NBC has also reached out to Kroger for more information about which states their product linked to the Caito recall were sold in. 

The USDA's Food Safety and Inspection Service stated that the potentially contaminated items were produced between July 15 and July 18 with either "Best By" or "Enjoy By" dates ranging from July 18 to July 23, 2018. The full public health alert issued by FSIS can be read here.

Consumers should throw any of the affected items away. 

Copyright Associated Press / NECN

Some Vanilla Almond Breeze May Contain Milk, Recall Issued

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HP Hood is recalling more than 145,000 half-gallon cartons of refrigerated Vanilla Almond Breeze almond milk because the products may contain milk – an allergen not listed on the label — according to the Food and Drug Administration

The company says the product is safe to drink unless consumers have a milk allergy or sensitivity. So far, there has only been one report of an allergic reaction to the product.

Almond milk is made with filtered water and almonds, among other ingredients

The products were shipped to retailers and wholesalers in a number of states including Connecticut, New York, Virginia, Florida, Texas, Illinois, Maryland, Pennsylvania, New Jersey, Missouri, Mississippi, Alabama, Arkansas, Michigan, Georgia, Iowa, Kentucky, Indiana, Louisiana, Maine, Nebraska, Minnesota, North Carolina, Ohio, Oklahoma, South Carolina, Tennessee and Wisconsin. 

The recall applies to products with a use-by date of September 2, 2018. 

The stamped information to identify affected products is: 

  • USE BY: SEP 02 18 (07:36 – 20:48) H5 L1 51-4109
  • USE BY: SEP 02 18 (07:36 – 20:48) H5 L2 51-4109
  • USE BY: SEP 02 18 (07:36 – 20:48) H6 L1 51-4109
  • USE BY: SEP 02 18 (07:36 – 20:48) H6 L2 51-4109

Additionally, products have a UPC bar code of 41570 05621 on the carton's side panel. 

Consumers can return affected containers to the store where it was purchased for a full refund or exchange. A web form can also be completed on the company's website



Photo Credit: Food and Drug Administration

FDA Expands Recalls of Blood Pressure, Heart Drugs

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The U.S. Food and Drug Administration has expanded its voluntary recall of several medications used to treat high blood pressure and heart failure over concerns that an active ingredient in the drugs could be contaminated with a cancer-causing agent.

The agency reported that traces of N-nitrosodimethylamine (NDMA), a "probable human carcinogen," was found in the active ingredient valsartan in the recalled products. The FDA noted not all products containing valsartan are contaminated and being recalled. A third-party supplied the valsartan contained in the recall. 

The FDA updated the list of products included in the recall and the list of those unaffected

"FDA is working with drug manufacturers to ensure future valsartan active pharmaceutical ingredients are not at risk of NDMA formation," the FDA said. "The agency reminds manufacturers to thoroughly evaluate their API manufacturing processes, and changes to those processes, to detect any unsafe impurities."

Patients are urged to look at the drug name and company name on the label of their prescription bottle to determine whether a specific product has been recalled. If the information is not on the bottle, patients should contact the pharmacy that dispensed the medicine to find out the company name.

If a patient is taking one of the recalled medicines, they should follow the recall instructions each specific company provided, which will be available on the FDA’s website.

If a patient's medicine is included in the recall, they should contact their health care professional to discuss their treatment options, which may include another valsartan product this recall doesn't affect or an alternative option.

The agency encourages patients and health care professionals to report any adverse reaction to the FDA’s MedWatch program.

"The FDA’s review is ongoing and has included investigating the levels of NDMA in the recalled products, assessing the possible effect on patients who have been taking them and what measures can be taken to reduce or eliminate the impurity from future batches produced by the company," the FDA said in a news release.

The presence of NDMA is "thought to be related to changes in the way the active substance was manufactured," the agency said.



Photo Credit: Joe Raedle/Getty Images

CVS Health Nasal Sprays Recalled Due to Contamination

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Certain bottles of CVS Health’s 12 Hour Sinus Relief Nasal Mist have been recalled after they were found to have had a microbiological contamination, the Food and Drug Administration said Wednesday.

The nasal mist, manufactured by Product Quest, was found to have Pseudomonas aeruginosa. Frequent use of the contaminated product could result in infections, which could be life-threatening for users with cystic fibrosis or people who are immuno-compromised, the FDA said on its website.

"To the best of Product Quest’s knowledge, the company has not received any reports of adverse events related to this recall," the FDA said.

The affected nasal sprays come in .5-ounce white bottles. They are packaged in a carton with expiration date September 2019 and lot number 173089J printed on the side. The products have orange labels with “Sinus Relief” in white letters and “CVS Health” in the left corner.

The FDA urges customers with the recalled product to return it to the store where it was purchased or to discard it.



Photo Credit: Food and Drug Administration

436 Confirmed Sick After Eating McDonald's Salad

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The CDC is now reporting that 436 people have been diagnosed with an intestinal illness after consuming salads at McDonald’s restaurants. 

The laboratory-confirmed cases of cyclosporiasis have been reported in 15 states after customers ate salads at the restaurant’s locations.

In its initial announcement July 13, the CDC reported 61 cases. As of last week, there were 395 cases. 

Over 200 cases have now been reported in Illinois and Iowa alone, with 219 cases confirmed in Illinois.  

The most common symptom of the illness is watery diarrhea. Other symptoms include appetite loss, intestinal pain, nausea, and fatigue.

McDonald's released a statement regarding the outbreak, saying "McDonald's is committed to the highest standards of food safety and quality control." 

Earlier this summer, McDonald’s removed the lettuce blend from 3,000 identified restaurants and distribution centers that had received it.

Affected restaurants were located in Illinois, Indiana, Iowa, Wisconsin, Michigan, Ohio, Minnesota, Nebraska, North Dakota, South Dakota, Montana, Kentucky, West Virginia, and Missouri. 

Reported illnesses started on or after May 20. 

In an update Thursday, the CDC said "at this time, there is no evidence to suggest that this cluster of illnesses is related to the Cyclospora outbreak linked to Del Monte fresh produce vegetable trays."



Photo Credit: AP

Allure Hair Dryer Recall Over Burn, Fire, Shock Hazards

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After receiving nearly 200 reports of Allure and Allure Pro ionic ceramic hair dryers exploding, catching fire, melting or overheating, the company that imported is recalling them and asking people not to use any until they are replaced.

Eighteen people who used the products were burned, one severely, and two people received minor electric shocks, according to a recall notice posted on the Consumer Product Safety Commission Wednesday. The company Xtava has received 193 reports of the product doing anything from overheating to exploding.

The recall affects about 235,000 units of the 2200W hair dryers, which were sold online since October 2014 for between $15 and $60 or as part of hair care kits that cost between $20 and $80.

Xtava, which imported the hair dryers from China, is offering free replacements. Click here for more information or contact the company at 877-643-8440 between 8 a.m. and 5 p.m. ET on weekdays.

The units have the word "xtava" imprinted near the blower and many bear the the SKU numbers XTV010001, XTV010001N, XTV010002 or XTV010002N.



Photo Credit: Xtava via CPSC

32 Children's Medicines Recalled Over Contamination Concerns

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King Bio is recalling 32 children's medicines due to a possible microbial contamination.

The North Carolina-based company, which makes homeopathic drugs, announced Wednesday that a small percentage of its products produced between Aug. 1, 2017 and April 2018 have tested positive for the microbial contamination.

The company said use of the medicines could result in increased or life-threatening infections. There have been no reports of illnesses, according to the FDA, and King Bio issued the recall "out of an abundance of caution."

The recalled products are used to treat dozens of conditions, including bed wetting, chicken pox, common colds, nosebleeds, sore throat and teething, and were sold nationwide between August 2017 and July 2018. 

Customers are urged to stop using the affected products immediately and contact King Bio by email at recall@kingbio.com or call the company at 866-298-2740, Monday through Friday from 8:30 a.m. ET to 3:30 p.m. ET., to make arrangements for a return and replacement of the product. Consumers who believe they may have been sickened by one of the recalled products should contact their physician or healthcare provider. 

All of the recalled products listed below come in 2-ounce bottles except for Kids Candida, which comes in a 4-ounce bottle. Products marked "SCRX" are only used by professionals. For a complete list of UPC and Lot numbers click here

• DK Attention & Learning Enh.
• Chicken Pox Symptom Relief
• Children's Appetite & Weight
• Children's Appetite Enhance
• Children's Cough Relief
• Children's Fever Reliever
• Children's Growth & Development
• DK Newborn Tonic
• DK Nosebleed Relief
• TonsilPlex
• Children's Ear Relief Formula
• DK Teething
• DK Colic Relief
• Tummy Aches
• Kids Multi-Strain Flu Relief
• Kids Stress & Anxiety
• Kids Sleep Aid
• Kids Bed Wetting (NP)
• Kids Candida - 4-ounce bottle
• Kids Attention & Learning (SCRX)
• Bed Wetting Prevention (SCRX)
• Chicken Pox Symptom Relief (SCRX)
• Childrens Cough (SCRX)
• Children’s Ear Formula (SCRX)
• Children’s Fever Reliever (SCRX)
• Children’s Growth & Development (SCRX)
• Colic Relief (SCRX)
• Newborn Tonic (SCRX)
• Teething (SCRX)
• Tummy Aches (SCRX)
• Children’s Apetite & Weight (SCRX)
• Children’s Appetite Enhancer (SCRX) 



Photo Credit: Dr. King's by King Bio

Vornado Reissues Space Heater Recall After Reports of More Fires, Death

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Vornado Air is reissuing its recall for thousands of electric space heaters after a man died in a fire involving one of the devices.

The company first recalled its VH101 Personal Vortex electric space heaters in April after receiving 15 reports of heaters that had caught on fire, according to a recall notice posted by on the Consumer Product Safety Commission's website. One person, a 90-year-old man from Minnesota, died in a fire involving the heater in December 2017, the notice said. 

A second recall notice issued Wednesday updates the number of reports the company has received of Vornado Air heaters catching fire to 19.

The recall includes around 350,000 black, coral orange, grayed jade, cinnamon, fig, ice white and red Vornado VH101 Personal Vortex electric space heaters. The model number, VH101, is printed on a label on the bottom of the heaters.

The faulty heaters were sold at Bed Bath & Beyond, Home Depot, Menards, Orchard Supply and Target stores nationwide, as well as online at Amazon.com, Target.com and Vornado.com from August 2009 through March 2018 for about $30.

Customers who have purchased the recalled heaters should stop using them and contact Vornado for a full refund or a free replacement, the notice said.

For more information, contact Vornado by phone at 855-215-5131 from 9 a.m. to 4 p.m. ET Monday through Friday or online at www.vornado.com and click on "Recalls" in the lower right corner of the homepage or www.vornado.com/recalls and click on the VH101 Personal Heater recall button for more information.



Photo Credit: Consumer Product Safety Commission

50 Adult Meds Added to National Recall With 32 Kids' Items

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King Bio has announced it is pulling all of its water-based products across all brands, amounting to more than 50 products intended to treat virtually every ailment from migraines to allergies, amid a national recall over concerns about possible purity issues.

The company's founder, Frank King, announced the expanded recall in a statement on the website Monday. Nearly three dozen children's medicines have already been recalled over the microbial contamination fears. 

King Bio, a North Carolina-based company that makes homeopathic drugs, first said last week that a small percentage of its products produced between Aug. 1, 2017 and April 2018 tested positive for the microbial contamination.

The company said use of the medicines could result in increased or life-threatening infections. There have been no reports of illnesses, according to the FDA, and King Bio issued the recall "out of an abundance of caution."

There were still no reported illnesses as of Monday, and King Bio said it was notifying its distributors and customers by letter to arrange for return and/or replacement of all the affected medicines.

The recalled products are used to treat dozens of conditions, including allergies, migraine, anxiety, bed wetting, chicken pox, common colds, nosebleeds, sore throat and teething. Products meant for use on pets are also being recalled. They were sold nationwide between August 2017 and July 2018.

"We are truly sorry for the inconvenience or concern our recall may have caused, but we felt this was the right thing to do to maintain your trust," King said in a statement. "Thank you for your continued loyalty and confidence in our King Bio products."

Customers are urged to stop using the affected products immediately and contact King Bio by email at recall@kingbio.com or call the company at 866-298-2740, Monday through Friday from 8:30 a.m. ET to 3:30 p.m. ET. Consumers who believe they may have been sickened by one of the recalled products should contact their physician or healthcare provider. 

See a list of 32 the affected kids' medicines below. For a complete list of UPC and Lot numbers click here. Find all the recalled adult medicines here.

• DK Attention & Learning Enh.
• Chicken Pox Symptom Relief
• Children's Appetite & Weight
• Children's Appetite Enhance
• Children's Cough Relief
• Children's Fever Reliever
• Children's Growth & Development
• DK Newborn Tonic
• DK Nosebleed Relief
• TonsilPlex
• Children's Ear Relief Formula
• DK Teething
• DK Colic Relief
• Tummy Aches
• Kids Multi-Strain Flu Relief
• Kids Stress & Anxiety
• Kids Sleep Aid
• Kids Bed Wetting (NP)
• Kids Candida - 4-ounce bottle
• Kids Attention & Learning (SCRX)
• Bed Wetting Prevention (SCRX)
• Chicken Pox Symptom Relief (SCRX)
• Childrens Cough (SCRX)
• Children’s Ear Formula (SCRX)
• Children’s Fever Reliever (SCRX)
• Children’s Growth & Development (SCRX)
• Colic Relief (SCRX)
• Newborn Tonic (SCRX)
• Teething (SCRX)
• Tummy Aches (SCRX)
• Children’s Apetite & Weight (SCRX)
• Children’s Appetite Enhancer (SCRX) 



Photo Credit: Dr. King's by King Bio

Children's Advil Recalled Over Label Mix-Up, Overdose Fears

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A children's Advil product is being recalled after consumers complained that the dosage instructions on the label are written in different units than what is on the dosage cup.

Pfizer Consumer Healthcare on Monday issued the recall for four-ounce bottles of bubble gum-flavored Children's Advil Suspension, which give instructions in milliliters but has a dosage cup marked in teaspoons, according to a voluntary recall notice posted on the company's website.

"Pfizer concluded that the use of the product with an unmatched dosage cup marked in teaspoons rather than milliliters has a chance of being associated with potential overdose," the notice says.

Pfizer didn't say whether anyone had been sickened due to the discrepancy. Ibuprofen overdose can lead to nausea, headache, vomiting, blurred vision, dizziness and drowsiness, according to the pharmaceutical company. NBC has reached out to Pfizer to learn if anyone has reported being sickened.

Anyone with with questions about the recall or who want to report someone being sickened can call 1-800-88-Advil (1-800-882-3845) between 9 a.m. and 5 p.m. on weekdays.

The recalled product was sold nationwide between May and June of 2018. It has a lot number of R51129 and an expiration date of 11/20.



Photo Credit: Pfizer Inc.

Accord Health Issues Recall of Hydrochlorothiazide Tablets

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Accord Healthcare Inc. is voluntarily recalling one lot (Lot PW05264 – 46632 Bottles, NDC 16729-182-01) of Hydrochlorothiazide tablets USP, 12.5 mg, because of a labeling mix-up. The medication is used to treat high blood pressure.

A 100 count bottle of Hydrochlorothiazide tablets USP 12.5 mg was found to contain 100 Spironolactone tablets USP 25 mg. That medication is typically used to treat patients with congestive heart failure, cirrhosis of the liver, essential hypertension and severe heart failure.

The company is asking any consumers in possession of the medication to return it to your pharmacy or health care provider for confirmation.

Consumers and pharmacies with questions regarding this recall can contact Accord Healthcare, Inc. by phone at 1-855-869-1081, fax: 1-817-868-5362 or e-mail at rxrecalls@inmar.com.



Photo Credit: Getty Images

Rubber Critter Toys Recalled for Excessive Lead Paint Levels

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Tens of thousands of rubber critter toys in the shapes of animals are being recalled for excessive lead levels in their orange and yellow paint. 

BSN Sports sold the 31,200 recalled units nationally through catalogues and online at Amazon.com, Athleticconnection.com, Bsnsports.com, Esportsonline.com and Usgames.com from February 2017 to June 2018, according to a recall notice posted Wednesday by the U.S. Consumer Product Safety Commission. 

The toys, which the notice says are "primarily used to play physical education tossing games," are shaped like an octopus, alligator, chicken, frog, pig, penguin or cow.

"Consumers should immediately take the recalled rubber critter toys away from children," the recall notice said.

Lead is especially dangerous to children because their bodies absorb the toxic element more than adults' bodies do, and a child's nervous system is also more sensitive to lead's effects, according to the Environmental Protection Agency.

The toys, which were made in China and imported and distributed by BSN Sports, sold for about $10 for an individual rubber critter or up to $145 for a set, according to recallrt.com/rubbercritters. Sets ranged from two to 24 critters. 

BSN Sports said it was contacting all known purchasers directly but those who bought the critters can also request a merchandise credit by calling 1-888-847-8816 between 7 a.m. and 6 p.m. CT on weekdays. Those who want refunds can also register at recallrtr.com/rubbercritters.



Photo Credit: BSN Sports
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