Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only,...

FDA Recall #D-0373-2024 — Class II — February 7, 2024

Recall #D-0373-2024 Date: February 7, 2024 Classification: Class II Status: Terminated

Product Description

Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only, Mfg: Pfizer Pharmaceuticals, NDC 60793-0701-10

Reason for Recall

cGMP Deviations: Products were stored outside the drug label specifications.

Recalling Firm

Mckesson Medical-Surgical Inc. Corporate Office — Richmond, VA

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

70 vials

Distribution

Product was distributed to three direct accounts in NM, AZ and UT.

Code Information

567951

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated