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FDA

Mass Man Posed As Medical Pro, Injected Clients With Black Market Botox, Sickening Several Mass Man Posed As Medical Pro, Injected Clients With Black Market Botox, Sickening Several
Mass Man Posed As Medical Pro, Injected Clients With Black Market Botox, Sickening Several A Massachusetts man admitted in federal court to giving clients illegal cosmetic injections that left several people seriously ill with botulism, prosecutors said. Rodrigo de Medeiros Siqueira, 33, of Quincy, pleaded guilty to misbranding a drug after shipment in interstate commerce with the intent to defraud or mislead, the US Attorney for the District of Massachusetts said.  Federal prosecutors said Siqueira operated Rodrigo Beauty Inc. and offered cosmetic injection procedures beginning around August 2022. Authorities said he was not licensed to prescribe, dispense, or administer pr…
Chocolate Recall Expands After More Bars Linked To Salmonella Concern Chocolate Recall Expands After More Bars Linked To Salmonella Concern
Chocolate Recall Expands After More Bars Linked To Salmonella Concern A nationwide recall of chocolate bars has quickly expanded to include eight flavors after federal officials found possible Salmonella contamination in additional products. The FDA said on Friday, Jan. 16, that Spring & Mulberry has extended its initial recall — first focused on its Mint Leaf chocolate bar — to include seven additional date-sweetened flavors. The newly recalled bars are Earl Grey, Lavender Rose, Mango Chili, Mixed Berry, Mulberry Fennel, Pecan Date, and Pure Dark Minis, in addition to Mint Leaf.  According to the FDA, the affected products were sold in stores and o…
6 Million Eggs Recalled Nationwide Over Salmonella Risk 6 Million Eggs Recalled Nationwide Over Salmonella Risk
6 Million Eggs Recalled Nationwide Over Salmonella Risk A widely sold line of brown eggs is being pulled from stores and kitchens nationwide after federal testing found multiple Salmonella strains at a processing plant.  The Food and Drug Administration (FDA) says the recall could widen as distribution tracking continues. Black Sheep Egg Company has voluntarily recalled more than six million eggs distributed between Wednesday, July 9 and Wednesday, Sept. 17. The action covers 12-count and 18-count cartons of Black Sheep Egg Company Free Range Large Grade A Brown Eggs with “Best By” dates from Aug. 22 to Oct. 31, 2025, and UPC codes 8600105…
Ben’s Original Rice Products Pulled Nationwide Over Stone Contamination Risk Ben’s Original Rice Products Pulled Nationwide Over Stone Contamination Risk
Ben’s Original Rice Products Pulled Nationwide Over Stone Contamination Risk Ben’s Original has issued a voluntary nationwide recall of select Ready Rice products after small, naturally occurring stones were discovered in a limited number of packages.  The company said the stones may cause oral or digestive tract injuries if eaten. The recall affects specific batches of Ben’s Original Long Grain White Rice, Whole Grain Brown Rice, and Long Grain & Wild Ready Rice distributed between August and September through retailers including Target, HEB, Amazon, United Markets, and Piggly Wiggly. Ben’s Original said in a statement: “This recall is limited only to th…
Frozen Spinach Pulled From Shelves Nationwide Over Listeria Concerns Frozen Spinach Pulled From Shelves Nationwide Over Listeria Concerns
Frozen Spinach Pulled From Shelves Nationwide Over Listeria Concerns A nationwide recall has been issued for frozen spinach after tests found possible Listeria contamination. Sno Pac Foods, based in Caledonia, Minnesota, announced the voluntary recall after testing by a supplier detected Listeria monocytogenes in a batch of bulk spinach used in its production.  The bacteria can cause serious, sometimes fatal infections in young children, older adults, and people with weakened immune systems.  Healthy individuals typically experience short-term symptoms such as high fever, severe headache, nausea, stiffness, abdominal pain, and diarrhea. The recal…
Recall Issued For Pasta Product Sold Nationwide Recall Issued For Pasta Product Sold Nationwide
Recall Issued For Pasta Product Sold Nationwide A frozen pasta sold under a popular national brand is being recalled after a key ingredient was flagged for possible contamination. Demers Food Group announced Wednesday, Oct. 1, that it is voluntarily recalling select Scott & Jon’s Shrimp Scampi with Linguini Bowls.  This recall follows a report from supplier Nate’s Fine Foods, which issued a recall of its linguini product for potential Listeria contamination. The Food and Drug Administration (FDA) posted the company’s announcement on Thursday, Oct. 2, as a consumer safety notice. The action applies only to specific lot codes of…
Nationwide Frozen Food Recall Expanded Nationwide Frozen Food Recall Expanded
Nationwide Frozen Food Recall Expanded A nationwide recall of frozen foods is expanding after additional products were flagged for possible Salmonella contamination. On Wednesday, Sept. 10, the US Food and Drug Administration (FDA) announced that Chetak LLC Group is broadening its voluntary recall to include more Deep-branded frozen vegetable and fruit products.  The company said the expanded action covers items manufactured on shared equipment between December 2024 and August 2025. The move follows testing that found Salmonella in several frozen vegetable lots, including Deep-brand Sprouted Mat (Moth), Sprouted Moong (Mun…
FDA Limits Access To New COVID-19 Vaccines: Here's What To Know FDA Limits Access To New COVID-19 Vaccines: Here's What To Know
FDA Limits Access To New Covid-19 Vaccines: Here's What To Know As fall approaches, the Food and Drug Administration has authorized updated COVID-19 vaccines from both Pfizer-BioNTech and Moderna, but with access limited to those most at risk for severe illness. On Wednesday, Aug. 27, the FDA approved the 2025-2026 formulas from both companies, each tailored to target the LP.8.1 sublineage — a new offshoot of the JN.1 Omicron variant — aligning the vaccines with the strains currently circulating in the US.  Pfizer-BioNTech’s COMIRNATY LP.8.1 is approved for adults 65 and older, as well as individuals ages 5 to 64 with at least one underlying health…
Froot Loops, Other Iconic Cereals To Lose Artificial Colors Under Kellogg’s Deal Froot Loops, Other Iconic Cereals To Lose Artificial Colors Under Kellogg’s Deal
Froot Loops, Other Iconic Cereals To Lose Artificial Colors Under Kellogg’s Deal Bowing to mounting consumer and regulatory pressure, Kellogg’s announced it will remove all artificial dyes from its breakfast cereals sold in the United States. The company said it will make the change by the end of 2027.  It's a move that will transform the look of some of America’s most iconic breakfast foods. The decision follows a legally binding agreement between Kellogg’s and the Texas Attorney General’s office.  This agreement investigated the company’s continued use of synthetic food colorings in the US, despite Kellogg’s having already removed them from cereals sold in…
Cookware Could Pose Lead Hazard, FDA Says: What To Know Cookware Could Pose Lead Hazard, FDA Says: What To Know
Cookware Could Pose Lead Hazard, FDA Says: What To Know Federal regulators are urging consumers to stop using certain cookware after tests revealed the products may leach dangerous levels of lead into food. The Food and Drug Administration (FDA) announced that some imported aluminum, brass, and aluminum-alloy cookware sold in the US has been found to release lead during cooking. This poses a potential health hazard. The agency said the problem involves products made from alloys known as Hindalium/Hindolium or Indalium/Indolium. Among the flagged products is a line of pots labeled “Kadai/Karahi Tiger White,” sold at Mannan Supermarket in Jamaica…
'Rodent Activity' Prompts Recall Of Cheese Product Sold In MA 'Rodent Activity' Prompts Recall Of Cheese Product Sold In MA
'Rodent Activity' Prompts Recall Of Cheese Product Sold In MA A cheesemaker is pulling one of its products from store shelves after federal inspectors found troubling conditions inside its facility. Quesito El Establo, located in Salem, New Hampshire, has recalled all of its Spanish Cheese (Quesito Colombiano).  This action follows an FDA inspection that uncovered the presence of rodents, signs of rodent activity, and other unsanitary conditions during manufacturing and storage. The cheese was distributed to retail stores in Massachusetts, primarily serving Hispanic/Latino customers. The FDA warns that rodent presence can carry a variety of hea…
Public Health Alert Issued For Ham Salad Products Sold Across Country Public Health Alert Issued For Ham Salad Products Sold Across Country
Public Health Alert Issued For Ham Salad Products Sold Across Country A public health alert has been issued for certain ready-to-eat ham salad products due to possible contamination with Listeria monocytogenes, a bacteria that can cause serious illness. The US Department of Agriculture’s Food Safety and Inspection Service (FSIS) says the alert involves FDA-regulated breadcrumb products used in the ham salads, which were recalled by Newly Weds Foods. The affected items include: 12-ounce tubs labeled “Reser’s Fine Foods Ham Salad” with sell-by dates of Sept. 1, 2025 5-pound tubs labeled “Molly’s Kitchen Ham Salad” with sell-by dates of Aug. 31, 2025 View produ…
Biden Was Taking Ambien Before 'Absolutely Horrible' Debate Performance Against Trump, Son Says Biden Was Taking Ambien Before 'Absolutely Horrible' Debate Performance Against Trump, Son Says
Biden Was Taking Ambien Before 'Absolutely Horrible' Debate Performance Against Trump, Son Says Hunter Biden alleges his father took a prescription sleep drug in the hours before President Joe Biden’s widely panned 2024 debate showdown with Donald Trump. The younger Biden told YouTube host Andrew Callaghan in a three‑hour Channel 5 interview posted Monday, July 21, he had been optimistic heading into the debate because the president had just notched bipartisan wins and delivered what supporters called a vibrant State of the Union. That confidence, he said, vanished onstage. “He’s 81 years old. He’s tired as (expletive deleted)," Hunter Biden to Callaghan. "They give him Ambien to be a…
Listeria Scare Leads To Recall Of Mushroom Product Listeria Scare Leads To Recall Of Mushroom Product
Listeria Scare Leads To Recall Of Mushroom Product A mushroom product distributed to a produce supplier and supermarket has been recalled following the detection of a dangerous foodborne pathogen. The recall, posted by the FDA on Saturday, July 12, involves 200-gram packages of “Needle Mushrooms” distributed by LLK Trading Inc., a company based in Linden, New Jersey. According to the notice, routine testing revealed the presence of Listeria monocytogenes, a bacterium that can cause serious illness in children, the elderly, pregnant women, and individuals with weakened immune systems.  Symptoms can include high fever, severe headache, …
Stores In East Coast States, Including MA, Hit With Recall Of Wegmans Chocolate Favorite Stores In East Coast States, Including MA, Hit With Recall Of Wegmans Chocolate Favorite
Stores In East Coast States, Including MA, Hit With Recall Of Wegmans Chocolate Favorite A chocolate product sold at Wegmans stores has been recalled, federal officials say. The recall, due to the presence of an undeclared milk allergen, affects Wegmans Semi-Sweet Chocolate Nonpareils, which were sold in 18.5-ounce plastic tubs with six affected lot codes.  The candies were distributed across stores in:  Delaware Maryland  Massachusetts,  North Carolina,  New Jersey,  New York,  Pennsylvania,  Virginia,  Washington, DC. According to the FDA, the product’s label did not disclose the presence of milk, which can pose a serious o…
Cough Syrup Recall Issued Nationwide Over Bacteria Risk Cough Syrup Recall Issued Nationwide Over Bacteria Risk
Cough Syrup Recall Issued Nationwide Over Bacteria Risk A popular over-the-counter cough syrup has been recalled across the US following a contamination alert and product stability issue. New York-based Medtech Products Inc., headquartered in Tarrytown, issued the voluntary recall for five lots of its 4-ounce Little Remedies honey cough syrup due to the presence of Bacillus cereus, a bacterium that can cause foodborne illness. The recall also cites loss of shelf stability as a contributing factor. Symptoms linked to Bacillus cereus exposure can include vomiting, diarrhea, and stomach cramps.  While illness is typically short-term in health…
Deaths Linked To Poppy Seeds, FDA Under Fire Over Hidden Danger In Your Pantry Deaths Linked To Poppy Seeds, FDA Under Fire Over Hidden Danger In Your Pantry
Deaths Linked To Poppy Seeds, FDA Under Fire Over Hidden Danger In Your Pantry Poppy seeds — a staple on bagels and in pastries — are at the center of a stunning public health scare that has already cost lives, the U.S. Food and Drug Administration (FDA) confirmed on Tuesday, April 8. The FDA has extended the public comment period for its Request for Information about poppy seed contamination after reports of adverse events, including respiratory arrest and death, were linked to the presence of opiate alkaloids — toxic substances naturally found in the poppy plant but not supposed to contaminate seeds FDA RFI Extension. The danger is not theoretical: at least 19 death…
Massive Cucumber Recall Expands To Include New Products Massive Cucumber Recall Expands To Include New Products
Massive Cucumber Recall Expands To Include New Products A cucumber-linked Salmonella outbreak that’s sickened dozens has now led to another round of product recalls. this time targeting fresh food trays and tubs sold across five states. TGD Cuts, LLC of Jessup, Maryland, announced it is voluntarily recalling several cucumber-containing products distributed under multiple brands.  The affected items — including pre-packaged salsas, salads, and produce trays — were made using cucumbers from Bedner Growers Inc., the same Florida-based supplier at the center of a nationwide recall and Salmonella outbreak that has sickened at least 45 people and…
Popular Allergy Drugs Have Unbearable Itching Side Effect, FDA Warns: What To Know Popular Allergy Drugs Have Unbearable Itching Side Effect, FDA Warns: What To Know
Popular Allergy Drugs Have Unbearable Itching Side Effect, FDA Warns: What To Know Some patients may suffer from unbearable itching across their entire body after stopping common allergy medications, health officials said. People who quit Zyrtec or Xyzal after using them daily for several weeks or longer have reported a rare but serious reaction known as pruritus. The Food and Drug Administration issued a warning about the condition on Friday, May 16. In 209 cases tracked by the FDA, many described intense itching that appeared within days and disrupted their daily lives. "Patients did not experience itching before starting the medicines," the FDA said. "Report…
COVID-19: FDA Says It Will Limit Who Can Get Future Booster Shots COVID-19: FDA Says It Will Limit Who Can Get Future Booster Shots
Covid-19: FDA Says It Will Limit Who Can Get Future Booster Shots In a significant shift in vaccination policy, the Trump administration has revealed that approval for seasonal COVID-19 shots will be restricted to certain groups. The Food and Drug Administration (FDA) says it will continue to approve boosters for those 65 and older as well as others at higher risk of severe disease. But it will require vaccine makers to conduct major new clinical trials on their effectiveness before approving them for wider use on the broader population.  The FDA’s revised framework, published in the New England Journal of Medicine on Tuesday, May 20, stat…
LASIK Blamed In Officer's Suicide: 'He Left A Note Saying It Took Everything From Him' LASIK Blamed In Officer's Suicide: 'He Left A Note Saying It Took Everything From Him'
Lasik Blamed In Officer's Suicide: 'He Left A Note Saying It Took Everything From Him' A Pennsylvania police officer’s suicide is raising urgent questions about the hidden risks of LASIK eye surgery, a procedure often marketed as safe, fast, and life-changing.  For 26-year-old Ryan Kingerski, it was all of those things — but not in the way he hoped. “It just … it ruined his life. Ruined it. Completely ruined his life in 12 seconds,” said his father, Tim Kingerski, in an interview with WTAE Pittsburgh. ‘Witty, Charming, Smart’ Ryan, of Monroeville, was described as joyful, loyal, and magnetic. A graduate of Duquesne University and Central Catholic High School, he served for th…
Toxic Metals Detected In Rice Brands Sold Across US, Report Finds Toxic Metals Detected In Rice Brands Sold Across US, Report Finds
Toxic Metals Detected In Rice Brands Sold Across US, Report Finds A new report is raising concerns about elevated levels of arsenic and other heavy metals in rice products sold across the United States. Healthy Babies Bright Futures, a nonprofit focused on children's health, tested 145 rice samples from stores in 20 metro areas and found arsenic in every single one.  More than one in four contained arsenic levels that exceeded the federal safety threshold for infant rice cereal. The report warns that rice is the top source of arsenic from solid foods in diets of children under 2, and a major concern during pregnancy — when the developing brain is mo…
Eye Drops May Be Contaminated, Sparking Recall Of 1.8M+ Bottles Eye Drops May Be Contaminated, Sparking Recall Of 1.8M+ Bottles
Eye Drops May Be Contaminated, Sparking Recall Of 1.8M+ Bottles More than 1.8 million eye drop bottles distributed nationwide are being recalled because the products may not be sterile. AvKARE issued the voluntary recall for 1,819,080 cartons of eye drops in 75,795 cases. The Tennessee company said an audit by the Food and Drug Administration found manufacturing violations at BRS Analytical Services, the firm responsible for producing the eye care products. The drops were sold under AvKARE's label and shipped between Friday, May 26, 2023, and Monday, April 21, 2025. The FDA classified this as a "Class II" recall, which mean…
Nationwide Recall Issued For Popular Yogurt Product Nationwide Recall Issued For Popular Yogurt Product
Nationwide Recall Issued For Popular Yogurt Product A widely sold refrigerated food item has been pulled from store shelves due to a labeling issue that could pose a serious health risk for certain consumers. Knockro Inc., based in Pennsylvania, is recalling its Bonya-branded low fat yogurt parfaits because they may contain almonds that are not listed on the label.  Almonds are considered a tree nut and can cause severe or even life-threatening allergic reactions in individuals with sensitivities. The product is sold in 12-ounce clear plastic cups with an expiration date of Monday, May 5. It was available in retail stores across the US…
Getting Inked? FDA Warns These Tattoo Inks Could Cause Rashes, Scarring, Infections Getting Inked? FDA Warns These Tattoo Inks Could Cause Rashes, Scarring, Infections
Getting Inked? FDA Warns These Tattoo Inks Could Cause Rashes, Scarring, Infections Planning your next tattoo? You may want to check the ink first. The FDA says two popular tattoo ink products could leave customers with infections — or worse. The US Food and Drug Administration (FDA) is warning tattoo artists, retailers, and customers to stop using and selling two popular Sacred Tattoo Ink products after testing revealed they were contaminated with harmful bacteria that could cause serious skin infections, federal officials announced. According to the FDA, tests confirmed that Raven Black and Sunny Daze tattoo inks, both sold under the Sacred Tattoo Ink brand, are contamin…
Recall Issued For Snack Mix Sold In MA Recall Issued For Snack Mix Sold In MA
Recall Issued For Snack Mix Sold In MA A snack mix sold in stores across the Northeast has been recalled following a new federal warning. The recall affects two package sizes of the “19th Hole Snack Mix” made by New England Village Foods, which was distributed to small grocery markets and convenience stores in New England, New York, and Pennsylvania, according to a notice issued Tuesday, May 6, by the FDA. The product may contain allergens that are not properly listed on the label, posing a potential health risk for consumers. No illnesses have been reported. The recalled snack mix was sold in 5-ounce and 10-ounce clear cups an…
This 'Over-The-Counter Medication' Will Soon Be Allowed In NJ Schools Without Doctor's Note This 'Over-The-Counter Medication' Will Soon Be Allowed In NJ Schools Without Doctor's Note
This 'Over-The-Counter Medication' Will Soon Be Allowed In NJ Schools Without Doctor's Note New Jersey students are finally allowed to use sunscreen, wear hats, and bring sunglasses to school—without needing a doctor’s note. On March 31, Gov. Phil Murphy signed a bill into law that requires school districts to permit students to use FDA-approved sunscreen and sun-protective clothing at school and during school-sponsored activities, as long as parents provide written permission, according to a press release from the governor’s office. Previously, sunscreen was classified as an over-the-counter medication, and many districts restricted its use without a medical note. The new law, sp…
'Enough Is Enough': RFK Jr. Slams Food Dyes In Fiery Press Conference 'Enough Is Enough': RFK Jr. Slams Food Dyes In Fiery Press Conference
'Enough Is Enough': RFK Jr. Slams Food Dyes In Fiery Press Conference A fiery press conference by Health and Human Services Secretary Robert F. Kennedy Jr. lit up the debate over artificial food dyes on Tuesday, April 22—drawing a hard line on consumer safety and demanding regulatory reform. The event focused on Red Dye 3, a controversial colorant used in many candies, and the broader issue of petroleum-based food dyes still found in everyday products. While the FDA banned Red Dye 3 in January under The Delaney Clause—a law prohibiting additives linked to cancer in animals—it simultaneously stated there's no known risk to humans, triggering widespread confusio…
Counterfeit Ozempic Seized By FDA, Drugmaker Warns About Fake Injection's Dangers Counterfeit Ozempic Seized By FDA, Drugmaker Warns About Fake Injection's Dangers
Counterfeit Ozempic Seized By FDA, Drugmaker Warns About Fake Injection's Dangers The maker of Ozempic and federal regulators are sending out warnings about counterfeit versions of the anti-diabetic drug after several hundred fake units were seized outside the authorized supply chain. The counterfeit products involve one milligram doses of the popular semaglutide injection, Novo Nordisk said in a news release on Monday, April 14. The counterfeit Ozempic was found with lot number "PAR0362" and serial numbers beginning with 51746517. While lot number PAR0362 is authentic, it becomes counterfeit only when combined with those eight serial digits. "As the inve…
Butter Beware: Bacteria Found In Cabot Creamery's Popular Product Butter Beware: Bacteria Found In Cabot Creamery's Popular Product
Butter Beware: Bacteria Found In Cabot Creamery's Popular Product Butter lovers, beware. Cabot Creamery’s premium butter is being recalled after testing revealed elevated levels of coliform bacteria, a possible indicator of fecal contamination, officials said. Agri-Mark Inc., the Vermont-based maker of Cabot products, issued a voluntary recall for its 8oz Extra Creamy Premium Butter, Sea Salted after finished product testing detected high levels of bacteria, according to a federal release issued Wednesday, April 9. Cabot butter packaging. Cabot Creamery The impacted butter is packaged as two 4-ounce sticks in a cardboard shell and can be identifie…
Chocolate Products Recalled Because They May Contain Small Stones Chocolate Products Recalled Because They May Contain Small Stones
Chocolate Products Recalled Because They May Contain Small Stones A sweet treat may come with a hard surprise. Tony’s Chocolonely is recalling two of its popular chocolate bars because they may contain small stones that made it into the product during almond harvesting and processing. The voluntary recall, announced Wednesday, April 2, affects seven lots of the brand’s 6.35-ounce Dark Chocolate Almond Sea Salt Bar and Everything Bar.  The products were distributed nationwide at retail stores and through the company’s website between Friday, Feb. 7, and Monday, March 24. According to the Food and Drug Administration (FDA), 12 complaints were reporte…