FDA Drug Moderate Class II Terminated

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

Reported: March 20, 2024 Initiated: February 7, 2024 #D-0373-2024

Product Description

Reason for Recall

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

Details

Recalling Firm: Mckesson Medical-Surgical Inc. Corporate Office
Units Affected: 70 vials
Distribution: Product was distributed to three direct accounts in NM, AZ and UT.
Location: Richmond, VA

Frequently Asked Questions

What product was recalled? ▼

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. Recalled by Mckesson Medical-Surgical Inc. Corporate Office. Units affected: 70 vials.

Why was this product recalled? ▼

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

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on March 20, 2024. Severity: Moderate. Recall number: D-0373-2024.