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US Food and Drug Administration

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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…

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by Zak Failla
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…

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by Zak Failla
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…

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by Joe Lombardi
Business
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. …

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by Zak Failla
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…

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by Joe Lombardi
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…

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by Zak Failla
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…

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by Michael Mashburn
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…

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by Cecilia Levine
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,"…

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by Zak Failla
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…

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by Ben Crnic
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…

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by Zak Failla
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…

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by Zak Failla
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…

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by Zak Failla
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…

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by Zak Failla