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Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Pilot COVID-19 At-Home Test - recalled due to Due to microbial contamination, USA

2 years ago •source fda.gov • details

SD Biosensor, Inc. is requesting that consumers stop using and dispose of specific Pilot COVID-19 At-Home Tests in the United States because potentially harmful bacteria were found in the tube with liquid inside (pouch 2 of the kits). The affected test kits were distributed by Roche Diagnostics… See more

#recall #medicaldevices #unitedstates

Recalls Pilot COVID-19 At-Home Test - recalled due to Due to microbial contamination SD Biosensor, Inc. is r... photo #1
312   Comments Comment

Recall notice

Akorn human & animal drug products update - recalled due to discontinuation of the Quality program, USA

2 years ago •source fda.gov • details

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

Recalls Akorn human & animal drug products update - recalled due to discontinuation of the Quality program T... photo #1
312   Comments Comment

Recall notice

Advil sold by Family Dollar – Recalled due to stored outside of label temperature, USA

2 years ago •source fda.gov • details

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

Recalls Advil sold by Family Dollar – Recalled due to stored outside of label temperature Family Dollar is i... photo #1
312   Comments Comment

Recall notice

Del Maguey Copitas-Artisan ceramicware cups - recalled due to exceed levels for leachable lead, USA

2 years ago •source fda.gov • details

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

Recalls Del Maguey Copitas-Artisan ceramicware cups - recalled due to exceed levels for leachable lead Del M... photo #1
312   Comments Comment

Recall notice

Mayne Pharma Inc. FENTANYL Buccal Tablets CII - recalled due to Safety updates omissions, USA

2 years ago •source fda.gov • details

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

Recalls Mayne Pharma Inc. FENTANYL Buccal Tablets CII - recalled due to Safety updates omissions Teva Pharma... photo #1
312   Comments Comment

Recall notice

TruVision Health Dietary Supplement Capsules - recalled due to unapproved Hordenine & octodrine, USA

2 years ago •source fda.gov • details

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

#recall #blood #drugs #unitedstates

Recalls TruVision Health Dietary Supplement Capsules - recalled due to unapproved Hordenine & octodrine TruV... photo #1
312   Comments Comment

Recall notice

Male enhancement capsules - recalled due to undeclared tadalafil & sildenafil, USA

2 years ago •source fda.gov • details

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

#blood #drugs #recall #unitedstates

Recalls Male enhancement capsules - recalled due to undeclared tadalafil & sildenafil Gear Isle is voluntari... photo #1
312   Comments Comment

Recall notice

Akorn human & animal drug products - recalled due to discontinuation of the Quality program, USA

2 years ago •source fda.gov • details

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

Recalls Akorn human & animal drug products - recalled due to discontinuation of the Quality program The Akor... photo #1
312   Comments Comment

Recall notice

Terry Naturally® Vitamin B & EuroMedica® Vitamin B complex - recalled due to Undeclared milk, USA

2 years ago •source fda.gov • details

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

#milkallergy #recall #unitedstates

Recalls Terry Naturally® Vitamin B & EuroMedica® Vitamin B complex - recalled due to Undeclared milk Pharma... photo #1
312   Comments Comment

Recall notice

Jarman’s Midwest Cleaning Systems Alcohol Antiseptic products Update - recalled due to Methanol, USA

2 years ago •source fda.gov • details

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

Recalls Jarman’s Midwest Cleaning Systems Alcohol Antiseptic products Update - recalled due to Methanol Jarm... photo #1
312   Comments Comment

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