FDAClass IIOctober 4, 2017

Sterile Water for Injection recall: Sterility Concern

Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc.…

Why was Sterile Water for Injection recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot: 63-075-DK Exp. FEB 2019

Product
Sterile Water for Injection, USP Single Dose 100 mL vials, Rx only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 USA for Genentech, Inc.…
Recalling firm
Pfizer Inc.
Quantity
18,725 vials
Distribution
Nationwide in the USA
Recall date
October 4, 2017
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls