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US Food and Drug Administration

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 …
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…
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…
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…
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…
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…
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,"…
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…
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…
$116M COVID Test Scam: Federal Grand Jury In NJ Indicts Ex-NYC Health Care Company CEO From CT $116M COVID Test Scam: Federal Grand Jury In NJ Indicts Ex-NYC Health Care Company CEO From CT
$116M COVID Test Scam: Federal Grand Jury In NJ Indicts Ex-nyc Health Care Company CEO From CT The former CEO of a New York-based health care company was charged with orchestrating a coronavirus rapid-test investment scam that fleeced victims of $116 million, federal authorities said. Marc Schessel, 62, of Greenwich, CT, had his company, SCWorx Corps, make bogus public claims that it was buying and selling at least 48 million COVID test kits that it never received, an indictment returned in U.S. District Court in Newark alleges. "The claims share price surged, rising by over 400 percent from approximately $2.25 per share to an intraday high of $14.88. per share," according to a relea…
NJ FEDS: Miracle-Aspirin Investment Scam Sends Long Island Man To Prison For 4½ Years NJ FEDS: Miracle-Aspirin Investment Scam Sends Long Island Man To Prison For 4½ Years
NJ Feds: Miracle-Aspirin Investment Scam Sends Long Island Man To Prison For 4½ Years A Long Island man must spend the next 4½ years in prison for scamming investors out of $3.5 million through what he claimed was a revolutionary new aspirin, federal authorities in New Jersey said. Donald A. Milne III, a 57-year-old repeat offender from Massapequa, defrauded more than 70 victims from throughout the country, U.S. Attorney Philip R. Sellinger said. All thought they'd invested in what he touted as a “fast-acting form of powdered aspirin that could instantly stop heart attacks and strokes," Sellinger said. Milne used the money instead for a Caribbean vacation, boating expe…
NJ Pet Food Manufacturer With 'Grossly Insanitary Conditions' Halts Production, FDA Says NJ Pet Food Manufacturer With 'Grossly Insanitary Conditions' Halts Production, FDA Says
NJ Pet Food Manufacturer With 'Grossly Insanitary Conditions' Halts Production, FDA Says A New Jersey-based pet food manufacturer has stopped sales after the U.S. Food and Drug Administration cited the company for operating under "grossly insanitary conditions." Bravo Packing, Inc., of Carney's Point, agreed to stop selling, manufacturing, and distributing raw pet food pending compliance with the Federal Food, Drug, and Cosmetic Act (FD&C Act). During inspections in 2019 and 2021, the FDA found evidence of significant food safety violations including grossly insanitary conditions and the failure to follow Current Good Manufacturing Practice (CGMP) regulations…
UPDATE: More Similac Baby Formula Recalled After Infant Dies, FDA Says UPDATE: More Similac Baby Formula Recalled After Infant Dies, FDA Says
Update: More Similac Baby Formula Recalled After Infant Dies, FDA Says Abbott Laboratories voluntarily expanded its recall of certain Similac PM 60/40 cans and cases after a second infant who was given the powdered baby formula died, the U.S. Food and Drug Administration said. Abbott had already recalled certain Alimentum, Similac and EleCare baby formulas made at the same company facility in Michigan after four infants were sickened by bacterial infections and one of them died. That baby's death, as well as the second one discovered on Monday, Feb. 28, could have been caused by Cronobacter sakazakii bacteria found in the formulas, which were distributed thro…
Faced With Death, Man Becomes First Human To Get Heart Transplant From Pig Faced With Death, Man Becomes First Human To Get Heart Transplant From Pig
Faced With Death, Man Becomes First Human To Get Heart Transplant From Pig David Bennett had two options: Die or get a heart transplant from a genetically-modified pig. The 57-year-old Maryland resident opted for the latter and is doing well days after the procedure. The transplant was performed by surgeons with the University of Maryland School of Medicine at the University of Maryland Medical Center. The patient, David Bennett, is being monitored over the next days and weeks to make sure the transplant continues to be a success. He was ineligible for a conventional heart transplant at UMMC as well as at several other leading transplant centers after a review o…
Metal Found In These Drinks Forces FDA Recall In CT, NY, NJ, PA Metal Found In These Drinks Forces FDA Recall In CT, NY, NJ, PA
Metal Found In These Drinks Forces FDA Recall In CT, NY, NJ, PA Metal fragments and washers found in Minute Maid and Coca-Cola products have forced the US Food and Drug Administration to issue a voluntary recall in eight states. The products were distributed in Pennsylvania, Connecticut, New York, North Carolina, Maryland, Virginia, Maine and New Jersey, according to the FDA. The recalled Minute Maid products, first reported by Food Safety News, are: Berry Punch: Date codes Jan0422 NP and Jan0522 NP, Batch 0010323455 and 0010259344 (recall F-0276-2022) Strawberry Lemonade: Date code: Jan0322 NP, Batch: 0010259346 (recall F-0277-2022) Fruit Punch: Date…
NY Con Man Admits Scamming $3.5M From Elderly Investors In NJ, Elsewhere For Heart Attack Pill NY Con Man Admits Scamming $3.5M From Elderly Investors In NJ, Elsewhere For Heart Attack Pill
NY Con Man Admits Scamming $3.5M From Elderly Investors In NJ, Elsewhere For Heart Attack Pill A convicted con artist from Long Island admitted in federal court in Trenton on Monday that he scammed investors in a purportedly revolutionary new aspirin -- most of them elderly -- out of $3.5 million that he used as his own personal piggybank. Donald A. Milne III, a 57-year-old repeat offender from Massapequa, defrauded more than 70 victims from throughout the country who though they'd invested in Instaprin, which he touted as a “fast-acting form of powdered aspirin that could instantly stop heart attacks and strokes," Acting U.S. Attorney Rachael A. Honig said. He used the money instead…
Anti-Vax Podcast Star Joe Rogan: ‘I GOT COVID’ Anti-Vax Podcast Star Joe Rogan: ‘I GOT COVID’
Anti-Vax Podcast Star Joe Rogan: ‘I GOT COVID’ Podcast star Joe Rogan – who was blasted by the Biden Administration earlier this year for telling young people not to get vaccinated -- told his millions of followers on Wednesday, "I GOT COVID." The Newark-born comedian, who hosts the hugely popular Spotify podcast "The Joe Rogan Experience," told his 13 million Instagram followers that he was using a drug that health experts have urged the public to avoid. Rogan, 54, said in the video (see below) that he has “fevers and sweats” and “threw the kitchen sink” at the illness – including monoclonal antibodies and ivermectin, which is ordinar…
Seasoning Products Recalled Due To Possible Salmonella Contamination Seasoning Products Recalled Due To Possible Salmonella Contamination
Seasoning Products Recalled Due To Possible Salmonella Contamination McCormick & Company, Inc. is recalling four of its seasoning products after routine testing found that they might be contaminated with salmonella. The US Food and Drug Administration posted the recall on Tuesday, July 27.  The following products are impacted by the recall: McCormick Perfect Pinch Italian Seasoning 1.31 oz bottle (Affected Date Codes: BEST BY MAY 26 24 K, BEST BY MAY 27 24 K, BEST BY JUN 04 24 K, BEST BY JUN 05 24 K) McCormick Perfect Pinch Italian Seasoning 2.25 oz bottle (Affected Date Codes: BEST BY JUN 30 24 H, BEST BY JUL 01 24 H) McCormick Culinary Italian S…
COVID-19: Pfizer Nearing Release Of Vaccine For Children Ages 12 -15, FDA Says COVID-19: Pfizer Nearing Release Of Vaccine For Children Ages 12 -15, FDA Says
Covid-19: Pfizer Nearing Release Of Vaccine For Children Ages 12 -15, FDA Says The U.S. Food and Drug Administration could authorize Pfizer-BioNTech's coronavirus vaccine for children ages 12 to 15 as early as next week, the New York Times reported on Monday, citing federal officials.  The timing could not be better for school districts that are resuming in-person instruction and hoping for a full return to normalcy next fall.  Vaccinating children is also a crucial element in achieving heard immunity and decreasing numbers of hospitalizations and deaths, The Times says.  While NJ, NY and CT positive rates have been dropping, other states including Pen…
CDC, FDA Call For Pause On Johnson & Johnson Vaccine CDC, FDA Call For Pause On Johnson & Johnson Vaccine
CDC, FDA Call For Pause On Johnson & Johnson Vaccine The US Centers for Disease Control and Prevention and the US Food and Drug Administration are calling for a pause on the use of Johnson & Johnson's COVID-19 vaccine due to six cases of "rare and severe" blood clot cases reported. All six cases occurred among women between 18 and 48, and symptoms occurred 6 to 13 days after vaccination, FDA officials said in a joint statement. More than 6.8 million doses of the one-dose vaccine had been administered in the U.S. All Pennsylvania teachers and administrators were given the J&J vaccine. Out of the 200,000 offered the vaccine a…
COVID-19: Millions Of J&J Doses Tossed After Factory Mixup COVID-19: Millions Of J&J Doses Tossed After Factory Mixup
Covid-19: Millions Of J&J Doses Tossed After Factory Mixup Millions of doses of the Johnson & Johnson COVID-19 vaccine were destroyed following a dosage mix-up at a production lab, prompting a delay in shipments to states. According to reports, employees at Emergent BioSolutions, a production facility in Baltimore that produces the vaccine, mixed up two ingredients, ruining approximately 15 million doses of the vaccine. Johnson & Johnson said in a statement that one batch of the drug substance at Emergent BioSolutions “did not meet quality standards” and was “never advanced to the filling and finishing stages of our manufacturing process.” …
COVID-19: Millions Of J&J Doses Thrown Away After Factory Mixup COVID-19: Millions Of J&J Doses Thrown Away After Factory Mixup
Covid-19: Millions Of J&J Doses Thrown Away After Factory Mixup Millions of doses of the Johnson & Johnson COVID-19 vaccine had to be destroyed after there was a dosage mix-up at a production lab, prompting a delay in shipments to states. According to reports, employees at Emergent BioSolutions, a production facility in Baltimore that produces the vaccine, mixed up two ingredients, ruining approximately 15 million doses of the vaccine. Emergent is one of several companies that Johnson & Johnson enlisted to speed up manufacturing of its recently approved vaccine, the company said. The Baltimore factory where the tainted vaccine ingredient was fou…