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Drugs

Updated:

Dr. Reddy’s Sapropterin Dihydrochloride Powder for Oral Solution - recalled due to decreased potency, USA

1 week ago •source www.fda.gov

Recall notice

Dr. Reddy's Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY, along with its subsidiaries together referred to as "Dr. Reddy's"), today announced that it is voluntarily recalling six (6) lots of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg to the consumer level due to … See More

#blood #recall #drugs #us

Dr. Reddy’s Sapropterin Dihydrochloride Powder for Oral Solution - recalled due to decreased potency photo #1
303

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

1 week ago •source www.fda.gov

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 #us

Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil photo #1
303

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

4 weeks ago •source www.fda.gov

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 #us

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance photo #1
303

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

1 month ago •source www.fda.gov

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 #us

AvKARE, LLC Atovaquone Oral Suspension - recalled due to potential Bacillus cereus contamination photo #1
303

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

1 month ago •source www.fda.gov

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 #us

AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence photo #1
304

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

1 month ago •source www.fda.gov

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 #us

Amneal Vancomycin Hydrochloride for Oral Solution - recalled due to super poteny risk photo #1
303

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

1 month ago •source www.fda.gov

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 #us

Dietary supplements for sexual enhancement - recalled due to undeclared drugs photo #1
288

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

1 month ago •source recalls-rappels.canada.ca

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 #ca

Equate and Nature's Bounty Folic Acid 1MG recalled due to exceeding intake limits photo #1
84

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

1 month ago •source www.fda.gov

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 #us

Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter photo #1
303

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

2 months ago •source www.fda.gov

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 #us

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance photo #1
303

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