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Safety Reports: Drugs

Updated: June 25, 2024 2:02 PM

Real Time Reports

Recall notice

Glenmark Potassium Chloride Extended Release Capsules - recalled due to Failed dissolution, USA

1 year ago •source fda.gov • details

Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ is voluntarily recalling 114 batches of Potassium Chloride Extended-Release Capsules, USP (750 mg) 10 mEq K, to the consumer level. The product is being recalled because of failed dissolution. The Potassium Chloride Extended-Release Capsules being recalled were distributed nationwide to wholesale,… See more

#drugs #unitedstates

Recalls Glenmark Potassium Chloride Extended Release Capsules - recalled due to Failed dissolution Glenmark... photo #1

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Recall notice

Suntegrity Sunscreen foundation - recalled due to higher than acceptable microbiological mold count, USA

1 year ago •source fda.gov • details

On May 24, 2024, Suntegrity Skincare initiated a voluntary recall of nine lots of Suntegrity Impeccable Skin Sunscreen Foundation (Multiple Shades) based on its discovery of a higher-than-acceptable microbiological mold count (Species: Aspergillus Sydowii). The product was distributed online by the company and nationwide via retail stores.… See more

#recall #drugs #unitedstates

Recalls Suntegrity Sunscreen foundation - recalled due to higher than acceptable microbiological mold count... photo #1

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Recall notice

StellaLife Inc. Homeopathic StellaLife Oral Care Products - recalled due to microbial contamination, USA

1 year ago •source fda.gov • details

HomeoCare Laboratories Inc. is voluntarily recalling two batches of Homeopathic StellaLife Oral Care Products manufactured in 2024 due to FDA findings of microbial contamination. This recall is to be performed at the consumer level. The affected products were manufactured at HomeoCare Laboratories, shipped nationwide to our customers,… See more

#recall #drugs #unitedstates

Recalls StellaLife Inc. Homeopathic StellaLife Oral Care Products - recalled due to microbial contamination... photo #1

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Recall notice

Sagent Docetaxel Injection, USP - recalled due to presence of particulate matter, USA

1 year ago •source fda.gov • details

Sagent Pharmaceuticals today announced the voluntary recall of two lots of Docetaxel Injection, USP to the User Level as the result of a customer complaint due to the potential presence of particulate matter from the stopper in the drug product. The product was distributed by Sagent Pharmaceuticals… See more

#recall #drugs #unitedstates

Recalls Sagent Docetaxel Injection, USP - recalled due to presence of particulate matter Sagent Pharmaceutic... photo #1

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Recall notice

Hospira Buprenorphine Hydrochloride Injection and Labetalol Hydrochloride Injection - recalled due to Packaging Defect, USA

1 year ago •source fda.gov • details

Hospira, Inc., a Pfizer company ("Pfizer"), is voluntarily recalling the lots listed in the table below of Buprenorphine Hydrochloride Injection CarpujectTM Units and Labetalol Hydrochloride Injection, USP CarpujectTM Units to the User level. The recall was initiated due to the potential for incomplete crimp seals; one customer… See more

#pfizer #recall #drugs #unitedstates

Recalls Hospira Buprenorphine Hydrochloride Injection and Labetalol Hydrochloride Injection - recalled due t... photo #1

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Recall notice

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

1 year ago •source fda.gov • details

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

#ketogummiesscam #scam #blood #recall #drugs #unitedstates

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

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Recall notice

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

1 year ago •source fda.gov • details

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

Recalls Schwinnng Herbal Dietary Supplement - recalled due to contamination with Nortadalafil STOP CLOPEZ CO... photo #1

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Recall notice

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

1 year ago •source fda.gov • details

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

Recalls Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance Honeywell Safety Products U... photo #1

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Recall notice

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

1 year ago •source fda.gov • details

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

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

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Recall notice

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

1 year ago •source fda.gov • details

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

Recalls AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence Eugia US LLC... photo #1

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Safety Reports: Drugs

Real Time Reports

Glenmark Potassium Chloride Extended Release Capsules - recalled due to Failed dissolution, USA

Suntegrity Sunscreen foundation - recalled due to higher than acceptable microbiological mold count, USA

StellaLife Inc. Homeopathic StellaLife Oral Care Products - recalled due to microbial contamination, USA

Sagent Docetaxel Injection, USP - recalled due to presence of particulate matter, USA

Hospira Buprenorphine Hydrochloride Injection and Labetalol Hydrochloride Injection - recalled due to Packaging Defect, USA

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

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

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