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
Reported: August 6, 2025 Initiated: July 10, 2025 #D-0544-2025
Product Description
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
Reason for Recall
CGMP Deviations; particulates identified during visual inspection
Details
- Recalling Firm
- Pfizer Inc.
- Units Affected
- 50,855 2 mL vials
- Distribution
- Nationwide in the USA
- Location
- New York, NY
Frequently Asked Questions
What product was recalled? ▼
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.. Units affected: 50,855 2 mL vials.
Why was this product recalled? ▼
CGMP Deviations; particulates identified during visual inspection
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 6, 2025. Severity: Moderate. Recall number: D-0544-2025.
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