WhichRecall
Class IIReported 2025-08-06

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

Recalled by Pfizer Inc.

Reason for Recall

CGMP Deviations; particulates identified during visual inspection

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Recall Number
D-0545-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-07-10
Reported
2025-08-06
Distribution
Nationwide in the USA
Code Info
Lots GT2598, GT2599, Exp 09/30/26; HK2909, Exp 02/28/27; HR9969, Exp 04/30/27; HR9984, Exp 08/31/27.
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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