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) 1.2 Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to cGMP Deviations: Products were stored outside the drug...
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 Mckesson Medical-Surgical Inc. Corporate Office directly.
Affected Products
Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only, Mfg: Pfizer Pharmaceuticals, NDC 60793-0701-10
Quantity: 70 vials
Why Was This Recalled?
cGMP Deviations: Products were stored outside the drug label specifications.
Where Was This Sold?
This product was distributed to 3 states: AZ, NM, UT
About Mckesson Medical-Surgical Inc. Corporate Office
Mckesson Medical-Surgical Inc. Corporate Office has 276 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report