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Safety Reports: Recall

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

Dynacare Baby Powder - recalled due to potential metal or chemical contaminant, USA

1 year ago •source fda.gov • details

Dynarex Corporation is recalling Dynacare Baby Powder because it has the potential to be contaminated with asbestos. The product was sent to distributors on or after March 11, 2024, by direct delivery in the following states: AL, AR, CO, IL, KY, NC, NJ, PA, TN, FL, WA,… See more

#recall #cosmetics #unitedstates

Recalls Dynacare Baby Powder - recalled due to potential metal or chemical contaminant Dynarex Corporation... photo #1

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Recall notice

Bestway Spa pumps recalled due to product overheating, United States

1 year ago •source cpsc.gov • details

The U.S. Consumer Product Safety Commission and Bestway (Hong Kong) International Ltd. have announced the recall of approximately 866,000 AirJet and HydroJet Spa Pumps because the product can overheat causing the plastic housing to ignite, posing a fire hazard. The recalled spa pumps were sold together with… See more

#recall #unitedstates

Recalls Bestway Spa pumps recalled due to product overheating The U.S. Consumer Product Safety Commission an... photo #1

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Recall notice

Breas Vivo 45 LS Ventilator - recalled due to formaldehyde exposure, USA

1 year ago •source fda.gov • details

Breas Medical initiated a U.S. nationwide correction of 8,186 Vivo 45 LS ventilator devices. Internal testing of the ventilator identified the potential for short term elevated levels of formaldehyde exposure to users under specific conditions.

Short term formaldehyde emissions may lead to adverse pulmonary or neurological effects… See more

#recall #medicaldevices #unitedstates

Recalls Breas Vivo 45 LS Ventilator - recalled due to formaldehyde exposure Breas Medical initiated a U.S. n... 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

#drugs #recall #unitedstates

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

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Recall notice

Abbott FreeStyle Libre® 3 sensors - recalled due to Sensors incorrect readings, USA

1 year ago •source fda.gov • details

Abbott has initiated a voluntary medical device correction for a small number of FreeStyle Libre® 3 sensors due to sensors may provide incorrect high glucose readings. The product was distributed in the United States during the first half of May 2024.

The FreeStyle Libre 3 system includes… See more

#recall #medicaldevices #unitedstates

Recalls Abbott FreeStyle Libre® 3 sensors - recalled due to Sensors incorrect readings Abbott has initiated... 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

Umary Hyaluronic Acid, Food Supplement - recalled due to Undeclared Drug Ingredients, USA

1 year ago •source fda.gov • details

Main Products, Inc. is voluntarily recalling all lots of "Umary Acido Hialuronico, Suplemento Alimenticio 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 cannot be marketed as dietary… See more

#vitamins #recall #unitedstates

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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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Safety Reports: Recall

Real Time Reports

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

Dynacare Baby Powder - recalled due to potential metal or chemical contaminant, USA

Bestway Spa pumps recalled due to product overheating, United States

Breas Vivo 45 LS Ventilator - recalled due to formaldehyde exposure, USA

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

Abbott FreeStyle Libre® 3 sensors - recalled due to Sensors incorrect readings, USA

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

Umary Hyaluronic Acid, Food Supplement - recalled due to Undeclared Drug Ingredients, USA

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

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