FDA Drug Recalls

Recalls / Class II

Class IID-1346-2022

Product

PF-0.125% Bupivacaine HCl Injection, USP, 625 mg/500 mL (1.25 mg/mL), 500 mL bag, packaged in 10 x 1 IV Bag per case, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th Street Extension, West Columbia, SC 29172; NDC 69374-970-05

Affected lot / code info
Lots: BH2003A, Exp. 8/19/2022; BH2011A, Exp. 11/9/2022

Why it was recalled

CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.

Recalling firm

Firm
Nephron Sterile Compounding Center LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
4500 12th Street Ext, West Columbia, South Carolina 29172-3025

Distribution

Quantity
2030 bags
Distribution pattern
Nationwide in the USA

Timeline

Recall initiated
2022-08-10
FDA classified
2022-08-16
Posted by FDA
2022-08-24
Terminated
2024-10-11
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1346-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.