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FDAFDA · Food and drugs·Recall number D-0545-2025

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

Published August 6, 2025 · Recall initiated: July 10, 2025

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

CGMP Deviations; particulates identified during visual inspection

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
BICILLIN L-A
Manufacturer
Pfizer Inc.
Distributor
Nationwide in the USA
Lot
Lots GT2598, GT2599, Exp 09/30/26; HK2909, Exp 02/28/27; HR9969, Exp 04/30/27; HR9984, Exp 08/31/27.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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