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US Food and Drug Administration

These Gummies Just Got Pulled From Shelves Nationwide These Gummies Just Got Pulled From Shelves Nationwide
These Gummies Just Got Pulled From Shelves Nationwide A batch of vitamin gummies sold under three popular brand names has been recalled nationwide due to the potential presence of an undeclared peanut allergen. The products — from Welby, Berkley Jensen, and VitaGlobe — were distributed on Amazon.com and at Aldi and BJ’s retail stores, as well as online through various sellers. Consumers with a peanut allergy are being urged to return or dispose of affected bottles. The recall covers one lot number — 248046601 — with an expiration date of October 2026. The undeclared allergen was flagged during routine testing conducted by Aldi, despite interna…
Contamination Fears Prompt Nationwide Mushroom Recall Contamination Fears Prompt Nationwide Mushroom Recall
Contamination Fears Prompt Nationwide Mushroom Recall A nationwide recall has been issued for mushrooms sold in stores across the country due to possible listeria contamination, according to federal health officials. The voluntary recall affects 200-gram packages of enoki mushrooms distributed by New York City-based Hofood99 Inc., located in Brooklyn, according to a release posted by the US Food and Drug Administration (FDA) on Wednesday, June 11. Authorities say the mushrooms may be contaminated with Listeria monocytogenes — a bacterium that can cause serious and sometimes fatal infections in young children, older adults, or people with weake…
45 Sickened, 16 Hospitalized As Salmonella Outbreak In Cucumbers Expands To 18 States 45 Sickened, 16 Hospitalized As Salmonella Outbreak In Cucumbers Expands To 18 States
45 Sickened, 16 Hospitalized As Salmonella Outbreak In Cucumbers Expands To 18 States A Salmonella outbreak linked to a cucumber producer has now expanded to 18 states with 45 illnesses and 16 hospitalizations now reported. The US Food and Drug Administration (FDA) issued a new recall for Bedner Growers cucumbers on Friday, May 30.  The recalled cucumbers, grown in Boynton Beach, Florida, and distributed by Fresh Start Produce Sales, were shipped to retailers, distribution centers, wholesalers, and food service dealers from Tuesday, April 29, to Monday, May 19. The products were labeled as either being “supers,” “selects,” or “plains." Target had issued…
Recall Issued For Baked Beans Sold In 23 States, Including NY Recall Issued For Baked Beans Sold In 23 States, Including NY
Recall Issued For Baked Beans Sold In 23 States, Including NY A new recall has been issued for a popular baked bean product distributed to retailers in more than 20 states. The beans, made by Vietti Food Group and sold under the Yellowstone brand, are being pulled due to the presence of an undeclared allergen. According to the US Food and Drug Administration (FDA), the product contains undeclared soy, posing a risk to individuals with a soy allergy or severe sensitivity. Consuming the affected product could lead to serious or life-threatening reactions, the FDA said. The recall involves 15-ounce cans of Yellowstone Brown Sugar Molasses Baked Beans wi…
Bread Recalled After Glass Found On Loaves In Maryland, 5 Other States, FDA Says Bread Recalled After Glass Found On Loaves In Maryland, 5 Other States, FDA Says
Bread Recalled After Glass Found On Loaves In Maryland, 5 Other States, FDA Says Check your freezer — a Maryland-based bakery has issued a multi-state bread recall after glass was found on top of frozen loaves, federal officials say. Three types of frozen bread shipped to Maryland, Pennsylvania, Connecticut, and three other states are being recalled after fragments of glass were discovered on top of the products, according to a new alert from the US Food and Drug Administration (FDA). The bread was produced by Upper Crust Bakery LP, headquartered on Holladay Tyler Road in Glenn Dale, Maryland. No injuries had been as of late April, officials said, but the firm voluntar…
Recall Issued For Salad Brand Sold At Trader Joe's In 18 States, Including NY Recall Issued For Salad Brand Sold At Trader Joe's In 18 States, Including NY
Recall Issued For Salad Brand Sold At Trader Joe's In 18 States, Including NY A brand of salad sold at Trader Joe’s locations in 18 states has been voluntarily recalled following the discovery of an undeclared allergen. According to a recall notice posted by the US Food and Drug Administration, a limited quantity of Trader Joe’s Sesame Miso Salad with Salmon may contain milk, which is not listed on the label.  The potential allergen is linked to a packaging mix-up in which 500 salad units were mistakenly shipped with parmesan cheese crumbles instead of the expected crispy onions. The product was distributed by Taylor Fresh Foods Illinois and affects only salads…
Recall Issued For Popular Snack Mix Sold In NY Recall Issued For Popular Snack Mix Sold In NY
Recall Issued For Popular Snack Mix Sold In NY A popular snack mix sold in the Northeast and other regions has been recalled due to a labeling issue that could pose a health risk for some consumers. New England Village Foods of Milford, New Hampshire, is recalling all lots of its 5-ounce and 10-ounce containers of New England Village Snacks “19th Hole Snack Mix” because they may contain undeclared almonds, according to the US Food and Drug Administration. The recall involves clear plastic cups and tubs with reclosable lids. The products were distributed to small independent grocery markets and convenience stores throughout New England, …
Recall Issued For Specialty Burger Product Sold At Caraluzzi's 4 Fairfield County Locales Recall Issued For Specialty Burger Product Sold At Caraluzzi's 4 Fairfield County Locales
Recall Issued For Specialty Burger Product Sold At Caraluzzi's 4 Fairfield County Locales A family-owned Connecticut supermarket chain has issued a recall for a specialty hamburger product that may pose a serious health risk to some customers. Caraluzzi’s Markets, based in Bethel, announced a recall of its 8-ounce Italian Style Seafood Burgers due to the presence of undeclared egg, a known allergen.  The product was sold at all four store locations in Fairfield County: Bethel, Wilton, Newtown and Danbury. People with an egg allergy or severe sensitivity are at risk of a serious or potentially life-threatening reaction if they consume the mislabeled burgers, the US Food and…
Mislabeled Decaf Coffee Recalled For Giving Drinkers That Caffeinated Jolt Mislabeled Decaf Coffee Recalled For Giving Drinkers That Caffeinated Jolt
Mislabeled Decaf Coffee Recalled For Giving Drinkers That Caffeinated Jolt This Traverse City coffee hits different. That's what some customers were saying after brewing the brand's cherry-flavored decaf coffee — only to discover it packed a serious caffeine punch. That's because the bags were mislabeled, according to the US Food and Drug Administration. In a consumer alert, the agency said that Our Family Traverse City Cherry Artificially Flavored Decaf Light Roast Ground Coffee, distributed by Coffee Roasters, was incorrectly labeled as decaffeinated but actually contained caffeine. Related: Tostitos Recalls Chips Sold in 13 States Suffolk, Virginia-based Ma…
Recall Issued For 75,000 Bottles Of Popular Creamer Due To Health Hazards Recall Issued For 75,000 Bottles Of Popular Creamer Due To Health Hazards
Recall Issued For 75,000 Bottles Of Popular Creamer Due To Health Hazards A popular coffee creamer has been recalled due to potential health risks, affecting thousands of bottles distributed across 31 states. International Delight has voluntarily recalled over 75,000 bottles of its coffee creamer after reports of spoilage and illness from consumers, according to the US Food and Drug Administration (FDA). The recall, initiated on Friday, Feb. 21, was classified as Class II by the FDA on Wednesday, March 12 — indicating that while health risks are not life-threatening, they could cause temporary or medically reversible issues. The recall affects two flavors of Int…
Recall Issued For Salad Kits Sold At These Supermarkets In Massachusetts Recall Issued For Salad Kits Sold At These Supermarkets In Massachusetts
Recall Issued For Salad Kits Sold At These Supermarkets In Massachusetts A recall has been issued for a brand of salad kits sold at supermarkets in the region. The Southwest Salad Kits are being due to the potential presence of undeclared fish and wheat allergens, which could pose a serious risk to those with allergies or severe sensitivities, according to a notice from the US Food and Drug Administration (FDA). The voluntary recall, announced by Little Leaf Farms, applies to a specific lot code of its Southwest Salad Kits produced during a single run on Wednesday, Feb. 19. The issue affects fewer than 20 individual salad kits that were incorrectly assembled dur…
Norovirus Outbreak Prompts Recall Of Oysters Sold In 15 States Norovirus Outbreak Prompts Recall Of Oysters Sold In 15 States
Norovirus Outbreak Prompts Recall Of Oysters Sold In 15 States New York, New Jersey, Pennsylvania and Washington DC residents are being urged to avoid consuming certain oysters after a recall linked to a norovirus outbreak, federal officials announced.  The contaminated oysters were sold under the brands Fanny Bay, Buckley Bay, and Royal Miyagi and harvested between Dec. 1 and Dec. 9, 2024, from British Columbia (BC), Canada, according to the U.S. Food and Drug Administration (FDA). The oysters, distributed by S&M Shellfish Co. of San Francisco, were shipped to retailers and restaurants across several states, including New Jersey, New York, Pe…
Recall Issued For Ready-To-Eat Produce Sold In NY Stores Over Potential Listeria Contamination Recall Issued For Ready-To-Eat Produce Sold In NY Stores Over Potential Listeria Contamination
Recall Issued For Ready-To-Eat Produce Sold In NY Stores Over Potential Listeria Contamination Ready-to-eat fruit and vegetable products sold in the parts of the Northeast are being recalled. Connecticut-based Gracie’s Kitchens Inc., located in New Haven, has issued the recall due to potential contamination with Listeria, a bacteria that can cause serious health risks, according to the US Food and Drug Administration (FDA). The recall involves products manufactured between Monday, Nov. 4 and Wednesday, Nov. 13, and sold under the Gracie’s Kitchens, King Kullen, and Wild By Nature brands.   The products were distributed to grocery stores in New York and Connecticut. Items …
Frozen Waffle Listeria Recall Expands To 14+ Grocery Store Brands Frozen Waffle Listeria Recall Expands To 14+ Grocery Store Brands
Frozen Waffle Listeria Recall Expands To 14+ Grocery Store Brands A massive voluntary recall has been issued for frozen waffles sold by over 14 different grocery store chains nationwide due to the potential contamination with Listeria monocytogenes, TreeHouse Foods, Inc. announced on Friday, Oct. 18. Over 500 varieties of frozen waffles manufactured by TreeHouse Foods and sold with the branding of major retailers such as Walmart's Great Value and Target's Good & Gather have been recalled because of possible Listeria.  As stated in the release: "Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections …
Walmart Issues Massive Recall For Juice Product Sold In 23 States, Including NY Walmart Issues Massive Recall For Juice Product Sold In 23 States, Including NY
Walmart Issues Massive Recall For Juice Product Sold In 23 States, Including NY Apple juice sold at Walmart has been recalled due to high arsenic levels. The US Food and Drug Administration says 9,535 cases of the company's  Great Value brand 100 percent apple juice were sold in six-packs of 8-ounce plastic bottles bearing this expiration date: Best if Used by DEC2824 CT89-6, and a UPC code of 0-78742-29655-5. According to the FDA, the product contains inorganic arsenic above the action level set in industry guidance (13.2 parts per billion). They were sold in 23 states: New York, New Jersey, Connecticut, Massachusetts, Pennsylvania, Virginia,…
FDA Investigates Microdosed Chocolate After 48 People Fall Ill, Including New Yorker FDA Investigates Microdosed Chocolate After 48 People Fall Ill, Including New Yorker
FDA Investigates Microdosed Chocolate After 48 People Fall Ill, Including New Yorker Health officials are investigating a previously-recalled brand of micro-dosed gummies, chocolates, and cones after dozens have been hospitalized and one potentially associated death has been recorded. On Tuesday, July 2, the US Food and Drug Administration (FDA) gave an update on the investigation of Diamond Shruumz brand microdose products, reporting that since the initial recall, 48 people have fallen ill from 24 states, including New York. The administration first announced the recall on June 7. The products (which come in chocolate, cones, and gummy form) were later found to contain m…
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…
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…
NY Companies Sold Adulterated, Misbranded Dietary Supplements, Feds Say NY Companies Sold Adulterated, Misbranded Dietary Supplements, Feds Say
NY 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…
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 …
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…
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…
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…
Restaurants, Stores Warned Not To Sell Contaminated Oysters From This Area In Northeast Restaurants, Stores Warned Not To Sell Contaminated Oysters From This Area In Northeast
Restaurants, Stores Warned Not To Sell Contaminated Oysters From This Area In Northeast 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…
Kale, Spinach, Collard Green Products Produced In MD Subject To Listeria Recall Kale, Spinach, Collard Green Products Produced In MD Subject To Listeria Recall
Kale, Spinach, Collard Green Products Produced In MD 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. …
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…
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…
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…
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…
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…
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…