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Safety Reports: Drugs

Updated: April 28, 2023 4:01 PM

Real Time Reports

Mayne Pharma Inc. FENTANYL Buccal Tablets CII - recalled due to Safety updates were omitted in the Product Insert, USA

2 years ago •source fda.gov • details

Recall notice

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

#drugs #recall #unitedstates

Mayne Pharma Inc. FENTANYL Buccal Tablets CII - recalled due to Safety updates omissions photo #1

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

2 years ago •source fda.gov • details

Recall notice

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

#drugs #recall #blood #unitedstates

TruVision Health Dietary Supplement Capsules - recalled due to unapproved Hordenine & octodrine photo #1

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Pro Power Knight Plus, NUX, and Dynamite Super Male enhancement capsules - recalled due to undeclared tadalafil & sildenafil, USA

2 years ago •source fda.gov • details

Recall notice

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

#recall #drugs #blood #unitedstates

Male enhancement capsules - recalled due to undeclared tadalafil & sildenafil photo #1

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

2 years ago •source fda.gov • details

Recall notice

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

#drugs #recall #unitedstates

Akorn human & animal drug products - recalled due to discontinuation of the Quality program photo #1

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

2 years ago •source fda.gov • details

Recall notice

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

#drugs #recall #unitedstates

Camber Atovaquone Oral Suspension, USP - recalled due to Bacillus cereus photo #1

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

2 years ago •source fda.gov • details

Recall notice

Ascend Laboratories LLC. is voluntarily recalling Dabigatran Etcxilate 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

#drugs #blood #unitedstates

Ascend Laboratories Dabigatran Etexilate Capsules - recalled due to Detection of N-Nitrosodimethylamine Impurity photo #1

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

2 years ago •source fda.gov • details

Recall notice

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

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

Dr Rima Recommends Nano Silver dietary supplement - recalled due to unsubstantiated health claims photo #1

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Purely Soothing 15% MSM Drops - recalled due to non-sterility, USA

2 years ago •source fda.gov • details

Recall notice

Pharmedica USA LLC is voluntarily recalling two lots of Purely Soothing, 15% MSM Drops to the consumer level. This product is being recalled due to non-sterility. To date, Pharmedica USA LLC has not received any reports of adverse events or illness related to this recalled product. Product… See more

#drugs #recall #unitedstates #ro-tel

Purely Soothing 15% MSM Drops - recalled due to non-sterility photo #1

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Apotex Brimonidine Tartrate Ophthalmic Solution, 0.15% - recalled due to lack of sterility, USA

2 years ago •source fda.gov • details

Recall notice

Apotex Corp., with the knowledge of the US FDA, is initiating a voluntary recall at the Consumer level for six (6) lots of Brimonidine Tartrate Ophthalmic Solution, 0.15% specified below. This recall is being initiated out of an abundance of caution due to cracks that have developed… See more

#drugs #recall #unitedstates #ro-tel

Apotex Brimonidine Tartrate Ophthalmic Solution, 0.15% - recalled due to lack of sterility photo #1

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Delsam Pharma’s Artificial Eye Ointment - recalled due to microbial contamination, USA

2 years ago •source fda.gov • details

Recall notice

Global Pharma Healthcare is voluntarily recalling Batch No. H29 of Artificial Eye Ointment, distributed by Delsam Pharma to the consumer level, due to possible microbial contamination. Additionally, some product packaging is leaking or may otherwise be compromised. The product was distributed nationwide in the United States, and… See more

#drugs #recall #unitedstates #ro-tel

Delsam Pharma’s Artificial Eye Ointment - recalled due to microbial contamination photo #1

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Safety Reports: Drugs

Real Time Reports

Mayne Pharma Inc. FENTANYL Buccal Tablets CII - recalled due to Safety updates were omitted in the Product Insert, USA

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

Pro Power Knight Plus, NUX, and Dynamite Super Male enhancement capsules - recalled due to undeclared tadalafil & sildenafil, USA

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

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

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

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

Purely Soothing 15% MSM Drops - recalled due to non-sterility, USA

Apotex Brimonidine Tartrate Ophthalmic Solution, 0.15% - recalled due to lack of sterility, USA

Delsam Pharma’s Artificial Eye Ointment - recalled due to microbial contamination, USA

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