Class II
Drug Recall: Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001. Made in Austria, Carton NDC - 60793-701-10,
Pfizer Inc. · July 10, 2025
Reason for Recall
CGMP Deviations; particulates identified during visual inspection
Product Description
Bicillin L-A (penicllin G benzathine injectable suspension), 1,200,000 units per 2 mL, 2 mL-vial, Rx Only, Distributed by Pfizer Inc., New York, NY 10001. Made in Austria, Carton NDC - 60793-701-10, Syringe NDC - 60793-701-02
Distribution
Nationwide in the USA
States Affected
NATIONWIDE
Quantity Affected
50,855 2 mL vials
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0544-2025
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.