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Safety Reports: Recall

Updated:

Family Dollar is initiating a voluntary retail level product recall of certain over-the-counter drug products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to certain stores on or around June 1, 2022 through March 31, 2023 due to product being stored… See more

#recall #familydollar #unitedstates

Del Maguey Co., New York, NY is conducting a voluntary recall of certain ceramicware cups called copitas – small artisan cups traditionally used for drinking mezcal – because they may exceed FDA guidance levels for leachable lead. The copitas were distributed free-of-charge to consumers at retail locations,… See more

#recall #drugs #unitedstates

Teva Pharmaceuticals USA, has initiated a voluntary nationwide recall of specific lots of various strengths of FENTANYL Buccal Tablets CII to the Consumer Level. Teva USA manufactured and labeled these product lots exclusively for Mayne Pharma Inc. under Mayne’s label. This recall has been initiated because safety… See more

#recall #drugs #unitedstates

TruVision Health LLC is recalling several dietary supplement products because they contain the unapproved dietary ingredients hordenine and/or octodrine/DMHA (1,5-Dimethylhexylamine).  The products were distributed throughout the US, Canada, Australia, New Zealand, Germany, Ireland and England.

Hordenine is possibly unsafe when taken by mouth and might cause stimulating… See more

#blood #recall #drugs #unitedstates

Gear Isle is voluntarily recalling several Male enhancement capsules (Brands: Pro Power Knight Plus, NUX, Dynamite Super) to the consumer level. FDA analysis has found the products to be tainted with sildenafil and tadalafil. Sildenafil and tadalafil are ingredients known as Phosphodiesterase Inhibitors (PDE-5) inhibitors found in… See more

#drugs #blood #recall #unitedstates

The Akorn Trustee is initiating a voluntary recall of various within-expiry human and animal products as a result of the closures and discontinuation of the Quality activities of these marketed products. The discontinuation of the Quality program means the company will not be able to support or… See more

#recall #drugs #unitedstates

Pharma, Inc. of Green Bay, WI is voluntarily recalling its Terry Naturally® BioActive Vitamin B™ 60 count and EuroMedica® Active B Complex 60 count products, because they may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or… See more

#recall #allergicreaction #unitedstates #allergen

Jarman’s Midwest Cleaning Systems, Inc. is voluntarily recalling all lots of Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution, SOFT HANDS Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-sterile Solution, and Isopropyl Alcohol Antiseptic 75% Topical Solution Hand Sanitizer Non-sterile Solution to the consumer level. FDA… See more

#recall #unitedstates

Abbott initiated a voluntary medical device correction in February to emphasize instructions for its FreeStyle Libre®, FreeStyle Libre® 14 day and FreeStyle Libre® 2 Readers in the United States due to a limited number of reports worldwide (0.0017%) from users over several years that their reader’s lithium-ion… See more

#recall #medicaldevices #unitedstates

Piscataway, NJ, Camber Pharmaceuticals, Inc. is voluntarily recalling lot # E220182 of Atovaquone Oral Suspension, USP 750mg/5mL to the Consumer/User level, due to the potential Bacillus cereus contamination in the product. This product was distributed Nationwide to Wholesalers, Distributors, Retail Pharmacies, and Mail Order Pharmacies. To date,… See more

#recall #drugs #unitedstates