Mckesson Medical-Surgical Inc. Corporate Office recalls Bicillin L-A (Penicillin G Benzathine) 1.2, MMU / 2 mL Injection Prefilled Syringe 2 mL, Rx only, Mfg: Pfizer
Mckesson recalls Pfizer's Bicillin L-A injections due to improper storage conditions. Affected products may have label deviations. Consumers should check NDC numbers and contact pharmacy for details.
Lower-risk recall
cGMP Deviations: Products were stored outside the drug label specifications.
Contact the company & request your remedy
What happened, in plain English
Mckesson is recalling Pfizer's Bicillin L-A penicillin injections because they were stored outside label specifications. This could lead to incorrect drug strength or safety issues if used improperly. Read more at govinfonow.com/recall/32827-bicillin-l-a-penicillin-g-benzathine-recall-storage-deviations-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/32827-bicillin-l-a-penicillin-g-benzathine-recall-storage-deviations-risk · Updated September 23, 2026 · FDA enforcement record: FDA #D-0373-2024
Cite this page
“Bicillin L-A Penicillin G Benzathine Recall: Storage Deviations Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32827-bicillin-l-a-penicillin-g-benzathine-recall-storage-deviations-risk. Based on FDA recall #D-0373-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0373-2024%22&limit=1).
Why it’s dangerous
The injections were stored outside the required temperature and humidity conditions specified on the drug label. This could cause the medication to degrade, potentially leading to incorrect dosing or reduced effectiveness.
Who’s affected
Prescription patients who received Bicillin L-A injections from pharmacies using the recalled product. Healthcare providers handling these injections may also be affected.
How to tell if you have this one
Check for NDC numbers 60793-0701-10 or 567951 on the product label. The product is a prescription-only penicillin injection sold by Pfizer under Mckesson.
- Brand
Mckesson Medical-Surgical- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Product was distributed to three direct accounts in NM, AZ and UT.
| Recall number | Product, codes & lots | NDC |
|---|---|---|
| D-0371-2024 | Rocuronium Bromide Injection, Preservative Free, 10 mg / mL, Multiple-Dose Vial 10 mL, Rx only, Mfg: Auromedics Pharma LLC, NDC 55150-226-10; 1064081 | 55150-225-05, 55150-226-10 |
| D-0372-2024 | Infuvite Adult Multiple vitamins injection, single-dose vial 5mL, Rx only, MFG: Baxter Healthcare Corp., NDC 54643-5649-01; 519644 | — |
| D-0373-2024 | 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; 567951 | — |
What to do — step by step
Check Product Label
Look for NDC numbers 60793-0701-10 or 567951 on the syringe packaging.
Questions people ask
Is this product safe to use?
The recall is due to storage issues, not immediate safety risks. If stored correctly, the product should be safe, but the recall ensures proper handling.
How do I know if I have the recalled product?
Check the NDC numbers 60793-0701-10 or 567951 on the syringe label. This product is prescription-only and sold by Pfizer through Mckesson.
What should I do if I have the recalled product?
Contact your pharmacy for guidance. The recall does not require immediate disposal but ensures proper storage and handling.
Contact Mckesson Medical-Surgical
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-0373-2024 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-0373-2024 from Mckesson Medical-Surgical. 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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Where this comes from
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.
- Official source: FDA Recall #D-0373-2024 (February 7, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0373-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.