FDAFDA · Food and drugs·Recall number D-1091-2017
0.9% Sodium Chloride Injection, USP in 1000 mL Single Dose Flexible Container, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC# 0409-7983-09
Published August 23, 2017 · Recall initiated: July 26, 2017
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
Presence of Particulate Matter; stainless steel
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- ICU Medical Inc
- Distributor
- Nationwide
- Lot
- Lot: 61-841-FW Exp. 01/01/2018
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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