D-1347-2022 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- August 24, 2022
- Initiation Date
- August 10, 2022
- Termination Date
- October 11, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 33,870 vials
Product Description
PF-Labetalol HCl Injection, USP, 20 mg/4 mL (5 mg/mL), One 4 mL Unit-Dose Vial, packaged in 30 x 4 mL Sterile Unit-dose Vials per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th Street Extension, West Columbia, SC 29172; NDC 69374-946-34
Reason for Recall
CGMP Deviations: Potential for cross-contamination due to product carryover during manufacturing.
Distribution Pattern
Nationwide in the USA
Code Information
Lot: LB2005A, Exp 3/2/2023