FDAFDA · Food and drugs·Recall number D-0287-2015
Sterile Water for Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7990-09.
Published December 3, 2014 · Recall initiated: October 14, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide, Puerto Rico, and U.S. Virgin Islands.
- Lot
- Lot# 36-084-JT; Exp.12/15
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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