drugs Class II Updated 2013-05-01

Hospira Inc. recalls Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 2

Recalled Product

Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL Single patient infusion vial, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-30.

Hazard / Issue

Presence of Particulate Matter: A single visible particulate was identified during a retain sample inspection.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 11-185-DJ*, 11-196-DJ*, Exp 1NOV2013; * may be followed by 01 or 02
View official government recall

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