Home / Recalls / Hospira Inc. / D-0836-2016

D-0836-2016 Class III Ongoing

Recalled by Hospira Inc. — Lake Forest, IL

Recall Details

Product Type: Drugs
Report Date: May 11, 2016
Initiation Date: March 15, 2016
Termination Date: N/A
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 103,600 vials

Product Description

Quelicin (Succinylcholine Chloride) Injection, USP 200 mg. (20 mg/mL), 10 mL Multiple-dose vial, packaged in 25 Unit vials per carton, Rx only, HOSPIRA, INC., LAKE FOREST, IL 60045 USA, NDC 0409-6629-02

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for the lot number and/or expiration date to be faded or missing from the primary label on the glass vial.

Distribution Pattern

Nationwide

Code Information

Lot 52-045-EV, Exp 07/1/2016

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