Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bicillin L-A (penicillin G benzathine injectable suspension) Recalled by Pfizer Inc. Due to CGMP Deviations; particulates identified during visual inspection
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Pfizer Inc. directly.
Affected Products
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
Quantity: 19,279 vials
Why Was This Recalled?
CGMP Deviations; particulates identified during visual inspection
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pfizer Inc.
Pfizer Inc. has 114 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report