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Safety Reports: Drugs

Updated:

Cipla Albuterol Sulfate Inhalation Aerosol, 90 mcg (200 MI)- recalled due to Failure to deliver the recommended dose, USA

11 months ago •source fda.gov • details

Recall notice

Cipla Limited (BSE: 500087; NSE: CIPLA EQ; and hereafter referred to as "Cipla"), today announced that its wholly-owned subsidiary Cipla US is voluntarily recalling six batches of Albuterol Sulfate Inhalation Aerosol, 90 mcg (200 Metered Inhalation) manufactured in November 2021 to the consumer level due to Failure… See more

#recall #drugs #us

Cipla Albuterol Sulfate Inhalation Aerosol- recalled due to Failure to deliver the recommended dose photo #1
321

Major Dronabinol and Ziprasidone Hydrochloride capsules- recalled due to labeling mix-up, USA

1 year ago •source fda.gov • details

Recall notice

The Harvard Drug Group, LLC d/b/a Major Pharmaceutical and Rugby Laboratories is initiating a voluntary recall of a single lot of Dronabinol Capsules, USP, 2.5 mg and Ziprasidone Hydrochloride Capsules, 20 mg to the consumer level. The Harvard Drug Group, LLC received a customer complaint from a… See more

#recall #drugs #us

Major Dronabinol and Ziprasidone Hydrochloride capsules- recalled due to labeling mix-up photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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

G-SUPRESS DX pediatric drops- recalled due to Incorrect Packaging photo #1
48

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

1 year 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

#recall #drugs #us

Akorn human & animal drug products update - recalled due to discontinuation of the Quality program photo #1
321

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

1 year ago •source fda.gov • details

Recall notice

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 #us

Del Maguey Copitas-Artisan ceramicware cups - recalled due to exceed levels for leachable lead photo #1
321

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

1 year 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 #us

Mayne Pharma Inc. FENTANYL Buccal Tablets CII - recalled due to Safety updates omissions photo #1
321

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

1 year 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

#blood #recall #drugs #us

TruVision Health Dietary Supplement Capsules - recalled due to unapproved Hordenine & octodrine photo #1
321

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

1 year 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

#blood #drugs #recall #us

Male enhancement capsules - recalled due to undeclared tadalafil & sildenafil photo #1
321

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

1 year 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

#recall #drugs #us

Akorn human & animal drug products - recalled due to discontinuation of the Quality program photo #1
321

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

1 year 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

#recall #drugs #us

Camber Atovaquone Oral Suspension, USP - recalled due to Bacillus cereus photo #1
321

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