Succinylcholine Chloride Injection, USP 200 mg (20 mg/mL) Quelicin Multiple-dose vial, 10 mL, For I.V. or I.M. use. a.) one vial (NDC: 0409-6629-02), b.) 25 vial carton (NDC: 0409-6629-25).
Reported: August 9, 2017 Initiated: June 15, 2017 #D-1048-2017
Product Description
Succinylcholine Chloride Injection, USP 200 mg (20 mg/mL) Quelicin Multiple-dose vial, 10 mL, For I.V. or I.M. use. a.) one vial (NDC: 0409-6629-02), b.) 25 vial carton (NDC: 0409-6629-25).
Reason for Recall
Lack of Sterility Assurance
Details
- Recalling Firm
- Hospira a Pfizer Company
- Units Affected
- 15,034,600 10 mL multiple dose use vials
- Distribution
- U.S. (including Puerto Rico), Dutch Antilles, Barbados, Canada, Philippines, Kuwait, and Singapore
- Location
- Rocky Mount, NC
Frequently Asked Questions
What product was recalled? ▼
Succinylcholine Chloride Injection, USP 200 mg (20 mg/mL) Quelicin Multiple-dose vial, 10 mL, For I.V. or I.M. use. a.) one vial (NDC: 0409-6629-02), b.) 25 vial carton (NDC: 0409-6629-25).. Recalled by Hospira a Pfizer Company. Units affected: 15,034,600 10 mL multiple dose use vials.
Why was this product recalled? ▼
Lack of Sterility Assurance
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 9, 2017. Severity: Moderate. Recall number: D-1048-2017.
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