FDAFDA · Food and drugs·Recall number D-1261-2014
Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 mL Single-dose Fliptop Vial, For IV use, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA
Published April 30, 2014 · Recall initiated: March 27, 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
Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot 22-127-DK
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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