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Safety Reports: Drugs

Updated:

Real Time Reports

Recall notice

Amneal Vancomycin Hydrochloride for Oral Solution - recalled due to super potency risk, USA

1 year ago •source fda.gov • details

Amneal Pharmaceuticals, LLC. Bridgewater, New Jersey (Amneal), is voluntarily recalling 4 lots (see table below) of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL packaged in 80 mL, 150 mL, or 300 mL pack sizes, to the Consumer Level. Some bottles may have been overfilled which can… See more

#recall #drugs #unitedstates

Recalls Amneal Vancomycin Hydrochloride for Oral Solution - recalled due to super poteny risk Amneal Pharmac... photo #1
312   Comments Comment

Recall notice

Pyramid Wholesale Dietary supplements for sexual enhancement - recalled due to Undeclared Sildenafil and/or Tadalafil, California, USA

1 year ago •source fda.gov • details

Pyramid Wholesale is issuing a recall of various brands of products sold as dietary supplements for sexual enhancement because they contain undeclared prescription drugs including Sildenafil (Viagra) and/or Tadalafil (Cialis). There have been no reports of injury or illness, to date. They were sold in bulk to… See more

#drugs #supplement #california #unitedstates

Recalls Dietary supplements for sexual enhancement - recalled due to undeclared drugs Pyramid Wholesale is i... photo #1
329   Comments Comment

Recall notice

Equate and Nature's Bounty Folic Acid 1MG recalled due to exceeding intake limits, Canada

1 year ago •source recalls-rappels.canada.ca • details

Several brands of folic acid tablets have been recalled in Canada due to concerns that affected lots may exceed the acceptable intake limit for N-nitroso-folic acid. The recall involves multiple brands distributed across the country.

-Affected products
Brand: Compliments FOLIC ACID 1MG, Product Name: FOLIC ACID 1MG,… See more

#equate #drugs #recall #canada

Recalls Equate and Nature's Bounty Folic Acid 1MG recalled due to exceeding intake limits Several brands of... photo #1
87   Comments Comment

Recall notice

Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter, USA

1 year ago •source fda.gov • details

Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulates in the product… See more

#recall #drugs #unitedstates

Recalls Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter Endo Interna... photo #1
312   Comments Comment

Recall notice

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance, USA

1 year ago •source fda.gov • details

Brassica Pharma Pvt. Ltd. is voluntarily recalling the Eye Ointment products listed below with expiration dates ranging from February 2024 to September 2025. The products are being recalled due to a lack of sterility assurance. These products were distributed nationwide to wholesalers, retailers, and via the product… See more

#drugs #cvspharmacy #recall #walmart #unitedstates

Recalls Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance Brassi... photo #1
312   Comments Comment

Recall notice

Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadalafil, USA

1 year ago •source fda.gov • details

"Today The World" is voluntarily recalling two lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules to the consumer level. FDA analysis has found the products to contain undeclared Tadalafil and Nortadalafil. Products were distributed online nationwide in the USA. To date, no… See more

#recall #drugs #unitedstates

Recalls Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadala... photo #1
312   Comments Comment

Recall notice

Arize male enhancement capsules - recalled due to undeclared Nortadalafil, USA

1 year ago •source fda.gov • details

"Today The World" is voluntarily recalling one lot of Arize Herbal Dietary Supplement capsules to the consumer level. FDA analysis has found the products to contain undeclared Nortadalafil. The product was distributed online via their website in the USA. To date, no adverse events have been reported.… See more

#recall #drugs #unitedstates

Recalls Arize male enhancement capsules - recalled due to undeclared Nortadalafil "Today The World” is volun... photo #1
312   Comments Comment

Recall notice

TING® 1% Tolnaftate Athlete's Foot Spray recalled due to Benzene presence, USA

1 year ago •source fda.gov • details

Insight Pharmaceuticals is voluntarily recalling two lots of TING® 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid to the consumer level due to elevated levels of benzene. The affected TING® 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid lots were distributed nationwide in the United States through… See more

#recall #drugs #unitedstates

Recalls TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence Insight Pharmaceuticals is... photo #1
312   Comments Comment

Recall notice

Neptune's Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tianeptine, USA

1 year ago •source fda.gov • details

Neptune Resources, LLC issues a voluntary recall of Neptune's Fix Elixir, Neptune's Fix Extra Strength Elixir, and Neptune's Fix Tablets Products Due to the Presence of Tianeptine. The products were distributed nationwide in the USA to wholesale and retail customers. Neptune Resources LLC's distribution channels have not… See more

#recall #drugs #unitedstates

Recalls Neptune’s Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tian... photo #1
312   Comments Comment

Recall notice

Zendedi dextroamphetamine sulfate tablets - recalled due to mislabeled package, USA

1 year ago •source fda.gov • details

Azurity Pharmaceuticals, Inc. is voluntarily recalling one lot (F230169A) of Zenzedi® CII (dextroamphetamine sulfate tablets, USP) 30 mg to the consumer level. The product is being recalled due to a report from a pharmacist in Nebraska who opened a bottle of Zenzedi® 30 mg tablets and found… See more

#recall #drugs #unitedstates

Recalls Zendedi dextroamphetamine sulfate tablets - recalled due to mislabeled package Azurity Pharmaceutica... photo #1
312   Comments Comment

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