drugs Class II Updated 2013-08-21

Hospira Inc. recalls Propofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100

Recalled Product

Propofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100 mL, Single patient infusion vial, RX only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-24; Propofol Injectable Emulsion, 500 mg/50 mL, 50 mL, Single patient infusion vial, RX only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-33

Hazard / Issue

Presence of Particulate Matter; single visible particulate was identified during a retain sample inspection identified as stainless steel

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot 07-950-DJ Exp. Date 1JUL2013, 10-101-DJ Exp. Date 1OCT2013, and 10-102-DJ Exp. Date 1OCT2013
View official government recall

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