US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 9, 2019 (7 years ago)

PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9%…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

GMP Deviations: potential glass contamination

What was recalled

PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride Injection-250 mL, Rx Only Total Dose: (500 mcg/312.5 mg)/250 mL, Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-530-25

Recalling firm
Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
Origin
SC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0148-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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