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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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Critical RiskFDA Drug
Medications & Supplements/Prescription Drugs

Pfizer Inc.: Vancomycin Hydrochloride for Injection Recalled Due to Glass Particulates

Agency Publication Date: December 20, 2017
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Summary

Pfizer is recalling approximately 102,500 vials of Vancomycin Hydrochloride for Injection, USP (750 mg). This sterile powder, which is a generic antibiotic used to treat serious bacterial infections, was found to contain glass particulate matter inside the vials. If this medication is administered, the glass particles can cause serious internal health issues such as blood clots, organ damage, or inflammation. This recall specifically affects Hospira brand vials distributed across the United States and Puerto Rico.

Risk

The presence of glass particles in an injectable medication poses a critical risk because the shards can travel through the bloodstream. This can lead to local irritation, inflammation of the veins, or life-threatening complications like the blockage of blood vessels (embolism) which can cause strokes or damage to the lungs and other organs.

What You Should Do

  1. Locate your medication and check the label for Vancomycin Hydrochloride for Injection, USP, 750 mg, distributed by Hospira, Inc. (NDC: 0409-6531-02).
  2. Check the vial for Lot Number 632153A with an expiration date of 03/18 (March 2018).
  3. If your medication matches the affected lot number, stop using it immediately and do not administer it to any patient.
  4. Contact your healthcare provider or pharmacist immediately to discuss alternative treatments and to report the affected product.
  5. Return any unused vials from the affected lot to the pharmacy or place of purchase for a refund and further instructions.
  6. Contact Pfizer/Hospira directly if you have questions regarding the return process or to report any adverse reactions.
  7. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

๐Ÿ’ฐFull Refund

Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Vancomycin Hydrochloride for Injection, USP (750 mg)
Model:
NDC: 0409-6531-02
Recall #: D-0123-2018
Lot Numbers:
632153A (Exp. 03/18)
Date Ranges: Expiration Date 03/18

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 78000
Status: Resolved
Manufacturer: Pfizer Inc.
Sold By: Hospitals; Pharmacies
Manufactured In: United States
Units Affected: 102,500 vials
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.