Recall: D-887-2013

Class II - Potentially Harmful

Class IIClassification

2013-05-25Initiated

TerminatedStatus

Hospira Inc.Firm

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

Reason

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

Distribution

Nationwide

Source: FDA drug enforcement report via openFDA (Voluntary: Firm initiated). If you take this product, talk to your pharmacist or doctor before stopping it.