Tag:

US Food and Drug Administration

Baltimore
Business
Supplements Sold Nationwide Being Recalled Due To Presence Of 'Gas Station Heroin' In Products Supplements Sold Nationwide Being Recalled Due To Presence Of 'Gas Station Heroin' In Products
Supplements Sold Nationwide Being Recalled Due To Presence Of 'Gas Station Heroin' In Products Federal Health officials are cautioning consumers to avoid certain products that may contain an ingredient known as "gas station heroin."  Neptune Resources LLC announced a voluntary recall of all lots of "Neptune's Fix Elixir," "Neptune's Fix Extra Strength Elixir," and Neptune's Fix Tablets due to the possible presence of tianeptine, the US Food and Drug Administration (FDA) announced. Tianeptine, which has been called "gas station heroin" by some, is not FDA-approved for any medical use, and its presence in the products prompted the nationwide recall. "The presence of tianepti…

SHARE

by Zak Failla
Carroll
Lifestyle
Contamination Concerns Prompt Nationwide Robitussin Cough Syrup Recall Contamination Concerns Prompt Nationwide Robitussin Cough Syrup Recall
Contamination Concerns Prompt Nationwide Robitussin Cough Syrup Recall Two types of Robitussin cough syrup products sold nationwide are being recalled due to potential microbial contamination, federal authorities announced. This week, New Jersey-based Haleon announced a recall of several lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult that could be contaminated, according to the US Food and Drug Administration (FDA). Recalled items include:  Four- and eight-ounce Robitussin Honey CF Max Day Adult with these lot numbers/expiration dates:  T18010 with an expiration date of Oct. 31, 2025; T08730 with an…

SHARE

by Zak Failla
Suffolk NY
Business
Hauppauge Companies Sold Adulterated, Misbranded Dietary Supplements, Feds Say Hauppauge Companies Sold Adulterated, Misbranded Dietary Supplements, Feds Say
Hauppauge Companies Sold Adulterated, Misbranded Dietary Supplements, Feds Say Federal regulators stepped in when a New York business owner allegedly sold dietary supplements that weren’t all they were cracked up to be. Mohammed Islam agreed to settle a civil complaint from the US Food and Drug Administration (FDA) in Brooklyn federal court on Monday, Dec. 18. The complaint, filed in October 2023, alleged that Islam’s Long Island-based companies – Total Body Nutrition, TBN Labs, and Loud Muscle Science – violated federal law by manufacturing and distributing adulterated and misbranded dietary supplements. Specifically, an investigation found that the companies failed…

SHARE

by Michael Mashburn
White Plains
Business
Applesauce Pouches May Have Been Intentionally Contaminated: FDA Applesauce Pouches May Have Been Intentionally Contaminated: FDA
Applesauce Pouches May Have Been Intentionally Contaminated: FDA Lead contamination from applesauce that sickened dozens of youngsters may have been an "intentional act," a US Food and Drug Administration (FDA) official said in a brand-new report. The WanaBana Apple Cinnamon Fruit Purée Pouches were distributed nationwide through online and retail stores. The products subject to the recall, along with lot codes, are: WanaBana apple cinnamon fruit puree pouches – including three packs of 2.5 oz. - with the following lot codes shown on this page from the (FDA). Schnucks-brand cinnamon-flavored applesauce pouches and variety pack, 90g pouches, were …

SHARE

by Joe Lombardi
Nassau
Business
Massive Eye Drop Recall Expands: 3 Products Added As List Hits 29; Here's New Rundown Massive Eye Drop Recall Expands: 3 Products Added As List Hits 29; Here's New Rundown
Massive Eye Drop Recall Expands: 3 Products Added As List Hits 29; Here's New Rundown Three new products have been added to a  recall of more than two dozen over-the-counter eye drops because of the risk of eye infections that may lead to vision loss or blindness. The now 29 products are from these brands: CVS Health, Leader (Cardinal Health), Rugby (Cardinal Health), Rite Aid, Target Up&Up, and Velocity Pharma. The alert comes after FDA investigators found bacterial contamination in critical drug production areas of a manufacturing facility. The list the US Food and Drug Administration (FDA) provided late last month five Cardinal Health, Inc. p…

SHARE

by Joe Lombardi
Capital District
News
COVID-19: FDA Approves Updated Booster Shots Targeting New Variants COVID-19: FDA Approves Updated Booster Shots Targeting New Variants
Covid-19: FDA Approves Updated Booster Shots Targeting New Variants Health officials are one step closer to rolling out updated COVID-19 vaccines just in time for a rise in cases heading into the fall and winter months. The US Food and Drug Administration (FDA) approved new vaccines on Monday, Sept. 11, that are meant to better target currently circulating COVID-19 variants and provide better protection against hospitalization and death, the agency announced. Monday’s move affects vaccines manufactured by Moderna and Pfizer. The updated mRNA vaccines are each approved for people ages 12 and older and are authorized under emergency use for children ages 6 mo…

SHARE

by Michael Mashburn
Arlington
News
Contaminated Oysters: FDA Warns Virginia Restaurants, Stores Warned To Not Sell Shellfish Contaminated Oysters: FDA Warns Virginia Restaurants, Stores Warned To Not Sell Shellfish
Contaminated Oysters: FDA Warns Virginia Restaurants, Stores Warned To Not Sell Shellfish cThe US Food and Drug Administration has advised consumers, restaurants, and retailers across several states in the Northeast to dispose of raw oysters harvested from the Groton Approved Area in New London County, CT between Monday, Aug. 28 and Wednesday, Aug. 30, officials announced on Tuesday, Sept. 5.  The affected raw oysters were sent to retailers and distributors in Connecticut, Massachusetts, New York, Pennsylvania, and Virginia, and may have even been sent further than these states, according to the FDA.  The advisory was issued after the Connecticut Department of Agr…

SHARE

by Ben Crnic
New London
News
Contaminated Oysters: Restaurants, Stores Warned To Not Sell Groton-Harvested Shellfish By FDA Contaminated Oysters: Restaurants, Stores Warned To Not Sell Groton-Harvested Shellfish By FDA
Contaminated Oysters: Restaurants, Stores Warned To Not Sell Groton-Harvested Shellfish By FDA Federal officials are warning restaurants and stores across the Northeast to stop selling oysters harvested from an area in Connecticut, as they may be contaminated with pathogens that cause food poisoning.  The US Food and Drug Administration has advised consumers, restaurants, and retailers across several states in the Northeast to dispose of raw oysters harvested from the Groton Approved Area in New London County between Monday, Aug. 28 and Wednesday, Aug. 30, officials announced on Tuesday, Sept. 5.  The affected raw oysters were sent to retailers and distributors in Connectic…

SHARE

by Ben Crnic
Howard
Business
Kale, Spinach, Collard Green Products Produced In Jessup Subject To Listeria Recall Kale, Spinach, Collard Green Products Produced In Jessup Subject To Listeria Recall
Kale, Spinach, Collard Green Products Produced In Jessup Subject To Listeria Recall A Maryland-based company announced a recall of kale and other similar products that were shipped up and down parts of the East Coast and could be contaminated with Listeria. Lancaster Foods is voluntarily recalling three brands of Robinson Fresh, Lancaster, and Giant brand kale, spinach, and collard green products after a random sample tested positive for Listeria monocytogenes by the New York Agriculture and Markets Food Safety Division. Items subject to the recall were distributed to retailers and distributors in Maryland, Massachusetts, New Jersey, New York, Virginia, and Pennsylvania. …

SHARE

by Zak Failla
Baltimore
News
COVID-19: Recall Issued For Brand Of Rapid Tests That Could Produce Inaccurate Results COVID-19: Recall Issued For Brand Of Rapid Tests That Could Produce Inaccurate Results
Covid-19: Recall Issued For Brand Of Rapid Tests That Could Produce Inaccurate Results A manufacturer has recalled more than 56,000 COVID-19 rapid tests because they could produce inaccurate results. Universal Meditech Inc. issued the recall for Skippack Medical Lab antigen tests because they were distributed without appropriate clearance or approval by the US Food and Drug Administration (FDA). The kits were made from October 2021 to December 2021 and distributed in January 2022. The following styles/models have been recalled: Name of Product: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit UDI: None Model: Cassette Products were distributed with “Sk…

SHARE

by Joe Lombardi
New Haven
News
COVID-19: Recall Issued For Brand Of Rapid Tests That Could Produce Inaccurate Results COVID-19: Recall Issued For Brand Of Rapid Tests That Could Produce Inaccurate Results
Covid-19: Recall Issued For Brand Of Rapid Tests That Could Produce Inaccurate Results A manufacturer has recalled more than 56,000 COVID-19 rapid tests because they could produce inaccurate results. Universal Meditech Inc. issued the recall for Skippack Medical Lab antigen tests because they were distributed without appropriate clearance or approval by the US Food and Drug Administration (FDA). The kits were made from October 2021 to December 2021 and distributed in January 2022. The following styles/models have been recalled: Name of Product: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit UDI: None Model: Cassette Products were distributed with “Sk…

SHARE

by Joe Lombardi
Carroll
News
Watch What You Eat: Maryland DOH Issues Advisory For Possibly Contaminated Mushrooms Watch What You Eat: Maryland DOH Issues Advisory For Possibly Contaminated Mushrooms
Watch What You Eat: Maryland DOH Issues Advisory For Possibly Contaminated Mushrooms A consumer advisory for certain mushrooms that may be contaminated with Listeria bacteria shipped stateside from China has been issued by the Maryland Department of Health. Enoki mushrooms that traveled from Shandong Youhe Biotechnology Co Ltd. in the Shandong Province in China have been collected and sampled by the Department of Health earlier this month and tested positive for the bacteria. According to health officials in Maryland, they are working with the US Food and Drug Administration (FDA) and other states to investigate the source of the contamination, which is not linked to a sepa…

SHARE

by Zak Failla
Montgomery PA
Police & Fire
Convicted NJ Wife-Killer Guilty Of Selling Phony Cancer Cure For Dogs In PA Convicted NJ Wife-Killer Guilty Of Selling Phony Cancer Cure For Dogs In PA
Convicted NJ Wife-Killer Guilty Of Selling Phony Cancer Cure For Dogs In PA A Montgomery County man who was convicted of killing his wife was found guilty in federal court of selling bogus cancer cures to desperate dog owners, authorities say.  Jonathan Nyce, a 73-year-old Collegeville resident who spent five years in prison for his wife's 2004 Hopewell Township murder is convicted of wire fraud and other counts related to his phony veterinary business, said US Attorney Jacqueline C. Romero in a statement Friday, Dec. 23.  According to evidence reviewed in court, created a series of companies under the names "Canine Care," "ACGT," and "CAGT" and claimed to sell ca…

SHARE

by Mac Bullock
Baltimore
Business
Wegmans Recalls Some Vegetable Products Due To Salmonella Concerns Wegmans Recalls Some Vegetable Products Due To Salmonella Concerns
Wegmans Recalls Some Vegetable Products Due To Salmonella Concerns Check your refrigerator. Wegmans has issued a voluntary recall on its products containing micro greens, sweet pea leaves, and cat grass due to concerns they may be contaminated with salmonella. The recall involves the following products: Wegmans Organic Baby Kale & Baby Spinach with Sweet Pea Leaves 5 oz (UPC: 0-77890-52377-3) with a best by date of 12/20/22 Wegmans Organic Farm & Orchard Micro Greens 1.75 oz (UPC: 0-77890-25036-5) with best by dates 12/17/22 and 12/24/22 Wegmans Organic Farm & Orchard Cat Grass (UPC: 0-77890-50938-8 The recalled productsFDA The recall…

SHARE

by Michael Mashburn
Rivertowns
Business
COVID-19: Recall Issued For Brand Of Over-Counter Tests That Could Give False Negative Results COVID-19: Recall Issued For Brand Of Over-Counter Tests That Could Give False Negative Results
Covid-19: Recall Issued For Brand Of Over-Counter Tests That Could Give False Negative Results A new recall has been issued for a brand of COVID-19 tests due to an increased chance that the tests may give false negative results Detect, Inc. is voluntarily recalling specific lots of the Detect COVID-19 Test, an over-the-counter test used to identify SARS-CoV-2 (the virus that causes COVID-19) in self-collected nasal swabs. The recall affects 11,102 tests shipped to customers from July 26, 2022, through Aug. 26, 2022, the company said. The test was granted Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) in October, 2021. There is an increased chance t…

SHARE

by Joe Lombardi
Nassau
News
Common Drug Shortage Hits US Common Drug Shortage Hits US
Common Drug Shortage Hits US There's a shortage of some commonly found medications as this cold and flu season is off to the worst start in more than a decade, according to the US Food and Drug Administration (FDA). According to VOX, the reason for the shortages could be either due a lack of raw materials or a problem at the manufacturing plant. The following drugs and medications might be more difficult to find on shelves this year, according to the FDA: Albuterol Sulfate Inhalational Solution: Caused by a high-demand for the drug at the onset of the COVID-19 pandemic, VOX says. Amoxicillin (Oral Powder for Suspensi…

SHARE

by Cecilia Levine
Alexandria
News
Common Drug Shortage Plagues US Common Drug Shortage Plagues US
Common Drug Shortage Plagues US This cold and flu season may be feel worse than others: There's a shortage in some commonly-found medication, according to the US Food and Drug Administration (FDA). According to VOX, the reason for the shortages could be either due a lack of raw materials or a problem at the manufacturing plant. The following drugs and medications might be more difficult to find on shelves this year, according to the FDA: Albuterol Sulfate Inhalational Solution: Caused by a high-demand for the drug at the onset of the COVID-19 pandemic, VOX says. Amoxicillin (Oral Powder for Suspension) Epinephrine Injec…

SHARE

by Cecilia Levine
Nassau
Business
Ho, Ho, No: Lidl Recalling Advent Calendars Due To Salmonella Contamination Scare Ho, Ho, No: Lidl Recalling Advent Calendars Due To Salmonella Contamination Scare
Ho, Ho, No: Lidl Recalling Advent Calendars Due To Salmonella Contamination Scare The countdown to Christmas got off to a rough start for Lidl, which announced a voluntary recall of certain advent calendars due to a fear of Salmonella contamination, according to the US Food and Drug Administration (FDA). Lidl US, which has more than 12,000 stores in 32 countries, announced that it will be recalling 8.4-ounce “Favorina-branded Advent Calendars (Premium Chocolate With a Creamy Filling)” due to the potential contamination. The recall was announced on Tuesday, Dec. 6. 
“This product is being voluntarily recalled due to potential Salmonella contamination," the FDA noted. "S…

SHARE

by Zak Failla
Carroll
Business
Ho, Ho, No: Lidl Recalling Advent Calendars Due To Salmonella Contamination Scare Ho, Ho, No: Lidl Recalling Advent Calendars Due To Salmonella Contamination Scare
Ho, Ho, No: Lidl Recalling Advent Calendars Due To Salmonella Contamination Scare The countdown to Christmas got off to a rough start for Virginia-based Lidl US, which announced a voluntary recall of certain advent calendars due to a fear of Salmonella contamination, according to the US Food and Drug Administration (FDA). Lidl US, which has more than 12,000 stores in 32 countries, announced that it will be recalling 8.4-ounce “Favorina-branded Advent Calendars (Premium Chocolate With a Creamy Filling)” due to the potential contamination. The recall was announced on Tuesday, Dec. 6. 
“This product is being voluntarily recalled due to potential Salmonella contamination,"…

SHARE

by Zak Failla
Baltimore
Business
Recall Issued Issued For Several Shampoo Products Due To Possible Cancer-Causing Agents Recall Issued Issued For Several Shampoo Products Due To Possible Cancer-Causing Agents
Recall Issued Issued For Several Shampoo Products Due To Possible Cancer-Causing Agents Several shampoo products are being recalled due to the presence of possible cancer-causing agents.  The US Food and Drug Administration has announced the recall of select dry shampoo aerosol products produced prior to October 2021 by Dove, Nexxus, Suave, TIGI (Rockaholic and Bed Head), and TRESemmé due to "potentially elevated levels of benzene," FDA officials said.  The recall was issued by Unilever on Tuesday, Oct. 18, the company that owns the brands of the recalled products.  A complete list of recalled products is available here. Benzene is classified as a carcino…

SHARE

by Ben Crnic
White Plains
Business
Recall Issued Issued For Several Shampoo Products Due To Possible Cancer-Causing Agents Recall Issued Issued For Several Shampoo Products Due To Possible Cancer-Causing Agents
Recall Issued Issued For Several Shampoo Products Due To Possible Cancer-Causing Agents Several shampoo products are being recalled due to the presence of possible cancer-causing agents.  The US Food and Drug Administration has announced the recall of select dry shampoo aerosol products produced prior to October 2021 by Dove, Nexxus, Suave, TIGI (Rockaholic and Bed Head), and TRESemmé due to "potentially elevated levels of benzene," FDA officials said.  The recall was issued by Unilever on Tuesday, Oct. 18, the company that owns the brands of the recalled products.  A complete list of recalled products is available here. Benzene is classified as a carcino…

SHARE

by Ben Crnic
Carroll
Lifestyle
Magnets Force FDA To Recall 17+ Million Masks Used With Sleep Apnea Machines Magnets Force FDA To Recall 17+ Million Masks Used With Sleep Apnea Machines
Magnets Force FDA To Recall 17+ Million Masks Used With Sleep Apnea Machines Millions of masks used with sleep apnea machines are being recalled due to safety issues that could impact certain medical devices, the US Food and Drug Administration (FDA) announced. Philips Respironics announced that it is recalling certain masks used with CPAP and Bi-Level positive airway pressure (Bi-PAP) machines due to a “serious safety concern.” In total, more than 17 million masks are subject to the recall. According to the FDA, the recalled masks have magnets that connect mask components to hold the BiPAP or CPAP devices in place. “The magnets can potentially affect the funct…

SHARE

by Zak Failla
Middlesex MA
News
Former Medford EMT Pleads Guilty To Messing With Fentanyl Vials: DOJ Former Medford EMT Pleads Guilty To Messing With Fentanyl Vials: DOJ
Former Medford EMT Pleads Guilty To Messing With Fentanyl Vials: DOJ A former Massachusetts EMT is facing up to 10 years in prison after pleading guilty to tampering with liquid fentanyl vials at her ambulance company, the US Attorney's Office for Massachusetts reports.  Candice Mangan, of Medford, was a part-time EMT who tampered with three fentanyl citrate vials by replacing the fentanyl citrate with saline, the office reports. This happened while Mangan was working in Needham on or about September 20, 2020.  Tampering with such vials could jeopardize patents' health, according to Fernando P. McMillan, special agent in charge of the U.S…

SHARE

by David Cifarelli
Port Chester
News
COVID-19: New Booster Shots Targeting Omicron Variant Approved By FDA COVID-19: New Booster Shots Targeting Omicron Variant Approved By FDA
Covid-19: New Booster Shots Targeting Omicron Variant Approved By FDA It’s time to roll up your sleeve and get another COVID-19 vaccine. On Wednesday, Aug. 31, the US Food and Drug Administration (FDA) approved updated versions of COVID booster shots made by Pfizer and Moderna that target the highly contagious BA.5 Omicron subvariant. The updated vaccine boosters are designed to give people broad protection against COVID and can help protect against severe illness, hospitalization, and death, the FDA said in a statement. Pfizer’s modified booster was authorized for people ages 12 and older, while Moderna’s shot was approved for those 18 and up. People who…

SHARE

by Michael Mashburn
Capital District
News
NY Health Commissioner Orders All Pharmacies To Carry Overdose Medication Naloxone NY Health Commissioner Orders All Pharmacies To Carry Overdose Medication Naloxone
NY Health Commissioner Orders All Pharmacies To Carry Overdose Medication Naloxone Pharmacies in New York will soon be required to carry and dispense naloxone, the medicine used to quickly reverse the life-threatening effects of an opioid overdose. The state’s health commissioner, Dr. Mary Bassett, issued a statewide standing order for all pharmacies to carry the medication and dispense it without a prescription beginning Monday, Aug. 15. “This is as close as we can get to naloxone being 'over the counter' without action being taken by the US Food and Drug Administration,” Bassett said. Often sold under the brand name Narcan, naloxone is easily administered and can help…

SHARE

by Michael Mashburn
Baltimore
Lifestyle
Coffee, Nutrition Drink Maker Issues National Recall Of 53 Products For Bacterial Contamination Coffee, Nutrition Drink Maker Issues National Recall Of 53 Products For Bacterial Contamination
Coffee, Nutrition Drink Maker Issues National Recall Of 53 Products For Bacterial Contamination A national recall has been issued for more than four dozen nutritional and beverage products due to the potential for microbial contamination, specifically from the Cronobacter sakazakii organism, officials announced. Lyon Magnus LLC announced that it will be recalling 53 products that were distributed across the country due to the possible contamination, which could lead to illnesses that may include fever, vomiting, and urinary tract infections, according to the US Food and Drug Administration (FDA). Lyons Magnus LLC (“Lyons Magnus” or the “Company”) today announced that it is volunta…

SHARE

by Zak Failla
Cecil
News
Companies Selling Honey Tainted With Drugs Used To Fight Erectile Dysfunction: FDA Companies Selling Honey Tainted With Drugs Used To Fight Erectile Dysfunction: FDA
Companies Selling Honey Tainted With Drugs Used To Fight Erectile Dysfunction: FDA The US Food and Drug Administration (FDA) issued warning letters to four companies that allegedly illegally sold honey-based products that could contain drug ingredients found in erectile dysfunction medication. Testing by the FDA found that products being sold throughout the East Coast could pose a significant health risk to consumers due to the presence of drug ingredients that can be found in Cialis (tadalafil) and Viagra (sildenafil). Officials noted that those drugs are used to treat erectile dysfunction and are “restricted to use under the supervision of licensed health care professio…

SHARE

by Zak Failla
Yorktown
News
COVID-19: Vaccines For Kids Under 5 Unanimously Recommended By Expert FDA Panel COVID-19: Vaccines For Kids Under 5 Unanimously Recommended By Expert FDA Panel
Covid-19: Vaccines For Kids Under 5 Unanimously Recommended By Expert FDA Panel Federal health officials are moving closer to authorizing COVID-19 vaccines for the youngest Americans. The US Food and Drug Administration (FDA) voted on Wednesday, June 15 to recommend authorizing both the Moderna and Pfizer COVID-19 vaccines for children between the ages of 6 months and 5 years old. On Wednesday, the agency’s independent panel of experts voted to recommend the vaccines - which are currently only available for Americans 5 years and older - for younger children. All 21 members of the FDA's Vaccines and Related Biological Products Advisory Committee unanimously voted to a…

SHARE

by Zak Failla
Carroll
News
COVID-19: Vaccines For Kids Under 5 Unanimously Recommended By Expert FDA Panel COVID-19: Vaccines For Kids Under 5 Unanimously Recommended By Expert FDA Panel
Covid-19: Vaccines For Kids Under 5 Unanimously Recommended By Expert FDA Panel Federal health officials are moving closer to authorizing COVID-19 vaccines for the youngest Americans. The US Food and Drug Administration (FDA) voted on Wednesday, June 15 to recommend authorizing both the Moderna and Pfizer COVID-19 vaccines for children between the ages of 6 months and 5 years old. On Wednesday, the agency’s independent panel of experts voted to recommend the vaccines - which are currently only available for Americans 5 years and older - for younger children. All 21 members of the FDA's Vaccines and Related Biological Products Advisory Committee unanimously voted to a…

SHARE

by Zak Failla
Rivertowns
Business
National Recall Issued For Rainbox Sprinkles Products National Recall Issued For Rainbox Sprinkles Products
National Recall Issued For Rainbox Sprinkles Products A popular rainbow sprinkle product is being recalled, according to federal health officials. Illinois-based Wilton Industries initiated a voluntary recall of certain lots of Rainbow Chip Crunch Sprinkles And Rainbow Sprinkles Mix that may contain milk and could still be on store shelves, the US Food and Drug Administration (FDA) issued an alert on Monday, June 6. Rainbow Chip Crunch SprinklesFDA According to the FDA, the undeclared allergen is not declared on the product label after the issue was discovered earlier this month. Recalled items include: Rainbow Chip Crunch Sprinkles wi…

SHARE

by Zak Failla
Carroll
Lifestyle
National Recall Issued For Rainbox Sprinkles Products National Recall Issued For Rainbox Sprinkles Products
National Recall Issued For Rainbox Sprinkles Products A popular rainbow sprinkle product is being recalled, according to federal health officials. Illinois-based Wilton Industries initiated a voluntary recall of certain lots of Rainbow Chip Crunch Sprinkles And Rainbow Sprinkles Mix that may contain milk and could still be on store shelves, the US Food and Drug Administration (FDA) issued an alert on Monday, June 6. Rainbow Chip Crunch SprinklesFDA According to the FDA, the undeclared allergen is not declared on the product label after the issue was discovered earlier this month. Recalled items include: Rainbow Chip Crunch Sprinkles wi…

SHARE

by Zak Failla