Pfizer Inc. recalls Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA.…
- Recall date
- August 30, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0123-2018
- FDA classification
- Class I
- Brand / firm
- Pfizer Inc.
- Sold / distributed
- Nationwide USA and Puerto Rico
Why it was recalled
Presence of Particulate Matter: glass particulate found in vial
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
Vancomycin Hydrochloride for Injection, USP. 750 mg. Sterile Powder. Rx Only. Hospira, Inc., Lake Forest, IL 60045 USA. NDC: 0409-6531-02
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