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

FDA recall notice · announced March 20, 2024 · Mckesson Medical-surgical Inc. Corporate Office

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The product

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

Reason for recall

cGMP Deviations: Products were stored outside the drug label specifications.

Notes

Distribution: Product was distributed to three direct accounts in NM, AZ and UT.
Lot/code information: 567951
Quantity: 70 vials
Status: Terminated
Products in this recall event:
- Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedics Pharma LLC, NDC 55150-226-10 (D-0371-2024)
- Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01 (D-0372-2024)
- 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 (D-0373-2024)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.