Class I · High risk Terminated
PROPOFOL Injectable Emulsion
Reason Presence of particulate matter
Propofol Injectable Emulsion
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Temperature Abuse: Products experienced uncontrolled temperature excursions during transit.
What was recalled
Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), 20 mL Single patient infusion vials, packaged in 5 Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-30.
- Recalling firm
- Hospira Inc.
- NDC code
- 0409-4699-30
- Origin
- IL, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0389-2015
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Propofol recalls
See all
Class I · High risk Terminated
Propofol Injectable Emulsion
Reason Presence of particulate matter: particulate identified as a beetle.
Class II · Moderate risk Terminated
Diprivan
Reason cGMP deviations: Temperature abuse
Class II · Moderate risk Terminated
Diprivan
Reason cGMP deviations: Temperature abuse
Class II · Moderate risk Terminated
Propofol Injectable Emulsion
Reason cGMP deviations: Temperature abuse
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