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Safety Reports: Drugs

Updated: September 19, 2024 3:25 PM

Real Time Reports

Recall notice

Bionpharma Atovaquone Oral Suspension - recalled due to Cohnella bacteria, United States

1 year ago •source fda.gov • details

Bionpharma Inc. is voluntarily recalling (1) a single batch of Atovaquone Oral Suspension at the consumer level. The product was found to be contaminated with Cohnella bacteria. The affected batch of product was manufactured at CoreRx, Inc. and shipped nationwide to customers between December 21, 2023, and… See more

#drugs #recall #unitedstates

Recalls Bionpharma Atovaquone Oral Suspension - recalled due to Cohnella bacteria Bionpharma Inc. is volunta... photo #1

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Recall notice

B. Braun 0.9% Sodium Chloride for Injection - recalled due to particulate matter and fluid leakage, USA

1 year ago •source fda.gov • details

B. Braun Medical Inc. (B. Braun), is voluntarily recalling two (2) lots of 0.9% Sodium Chloride for Injection USP 1000 mL in E3 containers. The voluntary recall has been initiated due to the potential for particulate matter and fluid leakage of the respective containers. The product was… See more

#recall #drugs #unitedstates

Recalls B. Braun 0.9% Sodium Chloride for Injection - recalled due to particulate matter and fluid leakage B... photo #1

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Recall notice

Baxter Heparin Sodium Chloride Injection - recalled due to elevated endotoxin levels, USA

1 year ago •source fda.gov • details

Baxter International Inc. is voluntarily recalling one lot of Heparin Sodium in 0.9% Sodium Chloride Injection to the consumer level due to the potential for elevated endotoxin levels based on issues related to the bacterial endotoxin test specific to lot number. This issue affects one lot of… See more

#recall #drugs #unitedstates

Recalls Baxter Heparin Sodium Chloride Injection - recalled due to elevated endotoxin levels Baxter Internat... photo #1

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Recall notice

Healthy Living Migraine Relief Tablets - recalled due to Mislabeling, USA

1 year ago •source fda.gov • details

Aurobindo Pharma USA, Inc., on behalf of AuroHealth, is voluntarily recalling one lot of Healthy Living Migraine Relief, Acetaminophen, Aspirin & Caffeine tablets to the consumer level due to the product missing the manufacturer label. The product was distributed through Amazon to be known within the US… See more

#drugs #recall #unitedstates

Recalls Healthy Living Migraine Relief Tablets - recalled due to Mislabeling Aurobindo Pharma USA, Inc., on... photo #1

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Recall notice

Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence, USA

1 year ago •source fda.gov • details

Hikma Pharmaceuticals USA, Inc. is voluntarily recalling one lot of Acetaminophen Injection to the consumer/user level. The product is being recalled due to the potential presence of a bag labeled Dexmedetomidine HCL Injection (400mcg/100mL) inside the overwrap that is labeled Acetaminophen Injection, 1000mg/100mL, (10mg/mL). The product was… See more

#recall #drugs #unitedstates

Recalls Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence Hikma Pharmaceuticals U... photo #1

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Recall notice

Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling, USA

1 year ago •source fda.gov • details

Endo USA, Inc. is voluntarily recalling one lot of Clonazepam Orally Disintegrating Tablets to the consumer level. The product lot is being recalled due to mislabeling where an incorrect strength appears on the cartons. The product lot was distributed through wholesale distributors to retail pharmacies nationwide.

Risk… See more

#recall #drugs #unitedstates

Recalls Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling Endo USA, Inc. is voluntarily... photo #1

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Recall notice

Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients, USA

1 year ago •source fda.gov • details

GURU INC. is voluntarily recalling Infla-650 Herbal Dietary Supplement Capsules, Lot No. IN-032, 700 mg to the consumer/user level. Infla-650 capsules has been found to be tainted with acetaminophen, diclofenac and phenylbutazone, which are not listed on the label. Products containing acetaminophen, diclofenac and phenylbutazone cannot be… See more

#drugs #recall #dietarysupplements #unitedstates

Recalls Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients GURU INC.... photo #1

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Recall notice

Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients, USA

1 year ago •source fda.gov • details

SoloVital.com is voluntarily recalling all lots of Umary Acido Hialuronica, Suplemento Alimenticio – 30 Capletas de 850mg to the consumer level. FDA laboratory analysis confirmed that UMARY has been found to be tainted with the drug ingredients, diclofenac and omeprazole. Products containing diclofenac and omeprazole drug cannot… See more

#recall #drugs #unitedstates

Recalls Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients SoloVital.com is volu... photo #1

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Recall notice

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

1 year ago •source fda.gov • details

American Health Packaging on behalf of BluePoint Laboratories is voluntarily recalling 21 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… See more

#recall #drugs #unitedstates

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Mirtazipine (aka: Remeron), Hawaii, USA

1 year ago •reported by user-ktkpg736 • details

I am a 62yr old with plenty of driving experience. I have never had a traffic ticket in my life. Within a day or two of using Mirtapine (Remeron,) my ears filled with extreme pressure. I could hear my every heart beat, loudly in my ears, as… See more

#drugs #hawaii #unitedstates

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Safety Reports: Drugs

Real Time Reports

Bionpharma Atovaquone Oral Suspension - recalled due to Cohnella bacteria, United States

B. Braun 0.9% Sodium Chloride for Injection - recalled due to particulate matter and fluid leakage, USA

Baxter Heparin Sodium Chloride Injection - recalled due to elevated endotoxin levels, USA

Healthy Living Migraine Relief Tablets - recalled due to Mislabeling, USA

Hikma Acetaminophen Injection - recalled due to Dexmedetomidine HCL presence, USA

Clonazepam Orally Disintegrating Tablets - recalled due to Mislabeling, USA

Infla-650 Herbal Dietary Supplement Capsules - recalled due to undeclared drug ingredients, USA

Umary Acido Hialuronica Capsules - recalled due to Undeclared Drug Ingredients, USA

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

Mirtazipine (aka: Remeron), Hawaii, USA

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