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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

Mylan Ampicillin for Injection Recalled for Foreign Matter

Agency Publication Date: September 23, 2022
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Summary

Viatris Inc. is recalling 3,931 cartons of Mylan Ampicillin for Injection, USP (ampicillin), an injectable antibiotic medication. The recall was issued after a single strand of hair was discovered inside one of the medication vials. These products were distributed nationwide throughout the United States.

Risk

Injecting a drug contaminated with foreign material such as hair can cause local irritation, inflammation, or serious systemic complications if the material travels through the bloodstream. While one complaint has been received, no injuries or illnesses have been reported to date.

What You Should Do

  1. The recalled products are 10-count cartons of Mylan Ampicillin for Injection, USP, 2 grams/vial, identified by NDC 67457-352-10 (carton) and NDC 67457-352-02 (vial). This recall specifically affects lot 7105130 with an expiration date of 9/2023.
  2. Stop using the recalled product immediately.
  3. Contact the manufacturer or your distributor to arrange for the return of any remaining stock.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

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: Ampicillin for Injection, USP, 2 grams/vialby Mylan
Variants: 2 grams/vial, 10 x 2 g vials per carton
Lot Numbers:
7105130 (Exp 9/2023)
NDC:
67457-352-02
67457-352-10

Recall #: D-1542-2022; Mylan Manufactured in India for: Mylan Institutional LLC

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90886
Status: Resolved
Manufacturer: Viatris Inc
Sold By: Mylan Institutional LLC; Wholesalers
Manufactured In: India, United States
Units Affected: 3,931 cartons
Distributed To: Nationwide

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.