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Fresenius Kabi USA Recalls
93 recalls on record · July 17, 2013 to July 29, 2026 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 24, 2013DrugsFDA
Fresenius Kabi USA, LLC recalls Oxytocin Injection, USP, (Synthetic), 10 USP Units/mL, for IV Infusion or IM Use, Rx Only, 1 mL vial, APP ) 10 USP Units
Hazard: Subpotent Drug; 15-month stability test station
July 17, 2013DrugsFDA
Fresenius Kabi USA, LLC recalls Folic Acid Injection, USP, 5 mg/mL, For IM, IV or SC Use, 10 mL, Multiple Dose Vial, Rx only, APP Pharmaceuticals, LLC,
Hazard: Failed Impurities/Degradation Specification
July 17, 2013DrugsFDA
Fresenius Kabi USA, LLC recalls Benztropine Mesylate Injection, USP, 2 mg/2 mL (1 mg/1 mL), 2 mL Single Dose Vial, Rx only, labeled as a) Manufactured f
Hazard: Presence of particulate matter: characterized as thin colorless flakes that are visually and chemically consistent with glass delamination observed in reserve sample vials