FDA recall record

Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop recall — FDA D-0184-2023

Presence of Particulate Matter: Glass particulate matter detected in injectable.

Class Iclassification
D-0184-2023official record ID
Feb 1, 2023report date

Recall record at a glance

Official recordD-0184-2023
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmPfizer Inc.
Report dateFeb 1, 2023
Recall initiation dateDec 22, 2022
Quantity89,700 vials
LocationNew York, NY, United States

Official product description

Vancomycin Hydrochloride for Injection, USP, 1.5 g/vial, Sterile powder, Single-dose Fliptop Vial, 10 vials per carton, Rx only, Distributed by: Hospira, Inc., Lake Forest, IL 60045. NDC Vial 0409-3515-11; NDC Carton 0409-3515-01

Why the product was recalled

Presence of Particulate Matter: Glass particulate matter detected in injectable.

Distribution information

USA nationwide and Puerto Rico

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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