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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Prescription Drugs

Rocuronium Bromide and Other Injectable Drugs Recalled for Improper Storage

Agency Publication Date: March 8, 2024
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Summary

Mckesson Medical-Surgical Inc. is recalling 70 vials each of Rocuronium Bromide (a muscle relaxant), Infuvite Adult (a multi-vitamin injection), and Bicillin L-A (a penicillin antibiotic). These medications were stored at temperatures outside of the manufacturer's required specifications. Storing drugs incorrectly can cause them to break down or lose their effectiveness before they are used on patients.

Risk

Drugs stored outside of label specifications may degrade or lose potency. This can lead to patients receiving an ineffective dose or potentially experiencing unexpected side effects from degraded chemical components.

What You Should Do

  1. This recall affects Rocuronium Bromide Injection (NDC 55150-226-10), Infuvite Adult Multiple vitamins (NDC 54643-5649-01), and Bicillin L-A (Penicillin G Benzathine) (NDC 60793-0701-10) distributed to direct accounts in NM, AZ, and UT.
  2. To identify the specific units, check for the following identification codes on the packaging: 1064081 (Rocuronium Bromide), 519644 (Infuvite Adult), or 567951 (Bicillin L-A).
  3. Stop using the recalled product immediately.
  4. Contact Mckesson Medical-Surgical Inc. or your distributor to arrange for the return of any remaining inventory.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Rocuronium Bromide Injection, Preservative Free (10 mg / mL)by Auromedics Pharma LLC
Variants: 10 mL Multiple-Dose Vial, Rx only
Lot Numbers:
1064081
NDC:
55150-226-10
Product: Infuvite Adult Multiple vitamins injectionby Baxter Healthcare Corp.
Variants: 5mL single-dose vial, Rx only
Lot Numbers:
519644
NDC:
54643-5649-01
Product: Bicillin L-A (Penicillin G Benzathine) 1.2 MMU / 2 mL Injectionby Pfizer Pharmaceuticals
Variants: 2 mL Prefilled Syringe, Rx only
Lot Numbers:
567951
NDC:
60793-0701-10

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93935
Status: Resolved
Manufacturer: Mckesson Medical-Surgical Inc. Corporate Office
Sold By: Direct accounts
Manufactured In: United States
Units Affected: 3 products (70 vials)
Distributed To: New Mexico, Arizona, Utah

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.