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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

G-SUPRESS DX pediatric drops- recalled due to Incorrect Packaging, Puerto Rico

2 years ago •source fda.gov • details

Novis PR LLC is voluntarily recalling Lot D20911 Exp 10/25 of G-Supress DX Pediatric Drops to the consumer level. Some cartons of the product have been found to contain incorrect product inside. Incorrect product inside is an anesthetic/analgesic and not a brand of Novis PR LLC. Lot… See more

#drugs #recall #puertorico

Recalls G-SUPRESS DX pediatric drops- recalled due to Incorrect Packaging Novis PR LLC is voluntarily recall... photo #1
48   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

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

#blood #recall #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

Camber Atovaquone Oral Suspension, USP - recalled due to Bacillus cereus, USA

2 years ago •source fda.gov • details

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

Recalls Camber Atovaquone Oral Suspension, USP - recalled due to Bacillus cereus Piscataway, NJ, Camber Phar... photo #1
312   Comments Comment

Recall notice

Ascend Laboratories Dabigatran Etexilate Capsules - recalled due to Detection of N-Nitrosodimethylamine Impurity, USA

2 years ago •source fda.gov • details

Ascend Laboratories LLC. is voluntarily recalling Dabigatran Etexilate Capsules. USP 75 mg and 150 mg to the consumer/user level due to the presence of a nitrosamine. N-nitroso-dabigatran, above the established Acceptable Daily Intake (ADI) level. The product lots were distributed nationwide to wholesalers, Distributors and Retailers (dispensers)… See more

#blood #drugs #unitedstates

Recalls Ascend Laboratories Dabigatran Etexilate Capsules - recalled due to Detection of N-Nitrosodimethyla... photo #1
312   Comments Comment

Recall notice

Dr Rima Recommends Nano Silver dietary supplement - recalled due to unsubstantiated health claims, USA

2 years ago •source fda.gov • details

CUSTOMERS OF NATURAL SOLUTIONS FOUNDATION (the “Foundation”) This is to inform you of a voluntary product recall involving the following Foundation product (the “Product”) “DR. RIMA RECOMMENDS NANO SILVER 10 PPM” The Product label is depicted for your reference and ease in identifying the Product. This recall… See more

#drugs #recall #unitedstates #sub #ro-tel

Recalls Dr Rima Recommends Nano Silver dietary supplement - recalled due to unsubstantiated health claims CU... photo #1
312   Comments Comment

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