Class II

Drug Recall: Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , S

Pfizer Inc. · July 10, 2025

Reason for Recall

CGMP Deviations; particulates identified during visual inspection

Product Description

Bicillin L-A (penicillin G benzathine injectable suspension), 2,400,000 units per 4 mL, 4ml-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001, Made in Austria, Carton NDC- 60793-702-10 , Syringe NDC-60793-702-04

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

19,279 vials

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0545-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.