FDAFDA · Food and drugs·Recall number D-315-2013
QUELICIN (succinylcholine chloride) Injection, USP, 200 mg (20 mg/mL) 10 mL, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, , NDC 0409-6629-02
Published May 15, 2013 · Recall initiated: February 26, 2013
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: Loose crimp applied to the fliptop vial.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- QUELICIN
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide and Puerto Rico
- Lot
- Lot 21-480-EV Exp.12/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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