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
Reported: May 15, 2013 Initiated: February 26, 2013 #D-315-2013
Product Description
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
Reason for Recall
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 139,200 vials
- Distribution
- Nationwide and Puerto Rico
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Hospira Inc.. Units affected: 139,200 vials.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 15, 2013. Severity: Moderate. Recall number: D-315-2013.
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