FDA recall record

Pfizer Sterile Water for Injection, USP Single Dose 100 mL vials recall — FDA D-1177-2017

Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.

Class IIclassification
D-1177-2017official record ID
Oct 4, 2017report date

Recall record at a glance

Official recordD-1177-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPfizer Inc.
Report dateOct 4, 2017
Recall initiation dateSep 1, 2017
Quantity18,725 vials
LocationNew York, NY, United States

Official product description

Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc., South San Francisco, CA 94080-4990. NDC 50242-901-24

Why the product was recalled

Non-Sterility: cracked or chipped glass at the neck of Sterile Water for Injection vials.

Distribution information

Nationwide in the USA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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

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