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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