Bicillin L-A recall: CGMP Deviations
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
Why was Bicillin L-A recalled?
cGMP Deviations: Products were stored outside the drug label specifications.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
567951
- 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
- Recalling firm
- Mckesson Medical-Surgical Inc. Corporate Office
- Quantity
- 70 vials
- Distribution
- Product was distributed to three direct accounts in NM, AZ and UT.
- Recall date
- March 20, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)