WhichRecall
Class IIReported 2025-08-06

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

Recalled by Pfizer Inc.

Reason for Recall

CGMP Deviations; particulates identified during visual inspection

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Recall Number
D-0544-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-07-10
Reported
2025-08-06
Distribution
Nationwide in the USA
Code Info
Lots: HJ3235, Exp 09/30/26; GL2954, HP6222, Exp, 01/31/27; HR9967, Exp 05/31/27; HP6232, LT5190,Exp 09/30/27; HP6228, Exp 10/31/27;
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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