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Safety Reports: Drugs

Updated: April 23, 2024 12:02 PM

Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil, USA

6 months ago •source fda.gov • details

Recall notice

STOP CLOPEZ CORP is voluntarily recalling one lot of Schwinnng capsules to the consumer level. FDA analysis has found the Schwinnng products to contain Nortadalafil. Nortadalafil is an active drug ingredient known for the treatment of male erectile dysfunction. The presence of Nortadalafil in Schwinnng capsules makes… See more

#recall #drugs #unitedstates

Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil photo #1

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Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA

7 months ago •source fda.gov • details

Recall notice

Honeywell Safety Products USA, Inc. is voluntarily recalling Fendall 2000 Non-Sterile Eyewash Cartridge for the Fendall 2000 Eyewash Station. This recall is being conducted at the industrial consumer level. Honeywell’s supplier of the Fendall 2000 Non-Sterile Eyewash Cartridge has been found to be non-compliant with current good… See more

#recall #drugs #unitedstates

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance photo #1

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AvKARE, LLC Atovaquone Oral Suspension - recalled due to potential Bacillus cereus contamination, USA

7 months ago •source fda.gov • details

Recall notice

AvKARE, LLC. is voluntarily recalling lot # AW0221A of Atovaquone Oral Suspension, USP 750mg/5mL to the Consumer/User level, due to the potential Bacillus cereus contamination in the product found during stability testing at a 3rd party lab. Atovaquone Oral Suspension, USP was distributed between 03/18/2024 through 03/21/2024… See more

#drugs #unitedstates

AvKARE, LLC Atovaquone Oral Suspension - recalled due to potential Bacillus cereus contamination photo #1

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AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence, USA

7 months ago •source fda.gov • details

Recall notice

Eugia US LLC (f/k/a AuroMedics Pharma LLC) has initiated a voluntary recall of lot number 3MC23011 of Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial) - 10mL Vial to the consumer level due to a customer product complaint for the presence of white particles floating… See more

#recall #drugs #unitedstates

AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence photo #1

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

7 months ago •source fda.gov • details

Recall notice

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

Amneal Vancomycin Hydrochloride for Oral Solution - recalled due to super poteny risk photo #1

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

8 months ago •source fda.gov • details

Recall notice

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

Dietary supplements for sexual enhancement - recalled due to undeclared drugs photo #1

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

8 months ago •source recalls-rappels.canada.ca • details

Recall notice

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

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

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

8 months ago •source fda.gov • details

Recall notice

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

Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter photo #1

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

8 months ago •source fda.gov • details

Recall notice

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

#cvspharmacy #recall #walmart #drugs #unitedstates

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance photo #1

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

9 months ago •source fda.gov • details

Recall notice

“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

Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadalafil photo #1

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Safety Reports: Drugs

Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil, USA

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA

AvKARE, LLC Atovaquone Oral Suspension - recalled due to potential Bacillus cereus contamination, USA

AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence, USA

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

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

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

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

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

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

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