Pfizer Inc. recalls Bicillin L-A (penicillin G benzathine injectable suspension)
See all recalls from Pfizer Inc. →Recalled Product
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
Hazard / Issue
CGMP Deviations; particulates identified during visual inspection
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lots GT2598, GT2599, Exp 09/30/26; HK2909, Exp 02/28/27; HR9969, Exp 04/30/27; HR9984, Exp 08/31/27.
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Bicillin L-A (penicillin G →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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