RecallDepth
Class II Terminated

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

This recall has been terminated (originally issued September 18, 2013).

Company
Hospira Inc.
Recall Initiated
August 14, 2013
Posted
September 18, 2013
Recall Number
D-932-2013
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
283,150 vials
Firm Location
Lake Forest, IL, United States
Official Source
View on FDA website ↗

Reason for Recall

Presence of Particulate Matter: Visible particulate embedded in the glass vial was observed and confirmed in a sample bottle during retain sample inspection.

Distribution

Nationwide

Lot / Code Info

Lot #: 24-461-DJ*, Exp 12/14; 26-543-DJ*, Exp 02/15; 27-555-DJ*, 27-559-DJ*, Exp 03/15; *lot number may be followed by 01

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