Pfizer recalls 1.2 million units of Bicillin L-A (penicillin G benzathine) due to particulates found during visual inspection. Affected products have specific NDC codes and expiration dates. Consumers should contact Pfizer for details.
CGMP Deviations; particulates identified during visual inspection
Pfizer is recalling 1.2 million units of Bicillin L-A injectable suspension because particulates were found during visual inspection. This could cause serious injury if injected, so affected users should stop using the product and contact Pfizer.
Particulates in the injectable suspension can cause serious injury, including tissue damage or infection, if injected. The particulates were identified during visual inspection of the product.
Prescription users of Bicillin L-A (penicillin G benzathine) who received the recalled vials. Healthcare providers and patients using the product are at risk of serious injury from particulates.
Check for vials labeled 'Bicillin L-A (penicillin G benzathine) 1,200,000 units per 2 mL' with NDC codes 60793-701-10 or 60793-701-02. Products were distributed with specific expiration dates and lots.
Immediately stop using the recalled Bicillin L-A vials as they contain particulates that could cause serious injury.
Pfizer recalled the product because particulates were identified during visual inspection, which could cause serious injury if injected.
Look for vials labeled 'Bicillin L-A (penicillin G benzathine) 1,200,000 units per 2 mL' with NDC codes 60793-701-10 or 60793-701-02.
Stop using the product immediately and contact Pfizer for further instructions.
We’ve drafted a message you can send Pfizer to request your refund or repair — edit it as you like.
Subject: Recall D-0544-2025 — Pfizer Pfizer Hello, I own a Pfizer that is covered by recall D-0544-2025 from Pfizer. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
