drugs Class II Updated 2012-06-20

Hospira, Inc. recalls Propofol Injectable Emulsion, 1%, (10mg/mL), packaged in a)

Recalled Product

Propofol Injectable Emulsion, 1%, (10mg/mL), packaged in a) 200 mg/20 mL, 5 Units x 20 mL Single patient infusion vials per carton (NDC 0409-4699-30); b) 1 g/100 mL, 10 Units x 100 mL Single patient infusion vials per carton (NDC 0409-4699-24); Rx only, Hospira, Inc., Lake Forest, IL 60045, USA.

Hazard / Issue

Presence of Particulate Matter: A single visible particulate was observed in a retention sample bottles identified as stainless steel

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: a) 03440DJ*, Exp 1MAR2013; b) 07947DJ, Exp 1JUL2013; 10134DJ, Exp 1OCT2013; Note: * the lot may be followed by 01.
View official government recall

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