US Drug Recall Register
Class I · High risk Terminated Initiated Apr 2, 2014 (12 years ago)

Propofol Injectable Emulsion

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Particulate Matter: A glass defect was found on the interior neck of the vial during a retain sample inspection where the glass vial contained visible embedded metallic particulate and free floating metallic particulates were also found in solution.

What was recalled

Propofol Injectable Emulsion, 1%, 200 mg/20 mL (10 mg/mL), For I.V. Administration, Rx Only, 20 mL vial, Contains Benzyl Alcohol, Hospira, Inc., Lake Forest, IL 60045 USA, 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-1547-2014

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 Alcohol recalls

See all
Class II · Moderate risk Ongoing

BD ChloraPrep Clear

Reason Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator

CareFusion 213, LLC NDC 54365-400-31 D-0690-2026
Class I · High risk Ongoing

Glutathione

Reason Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

Victory Medical Center Pharmacy D-0772-2026
Class II · Moderate risk Ongoing

BD ChloraPrep CLear

Reason Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

CareFusion 213, LLC NDC 54365-400-34 D-0652-2026
Class II · Moderate risk Ongoing

BD ChloraPrep CLear

Reason Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

CareFusion 213, LLC NDC 54365-400-31 D-0651-2026
Class II · Moderate risk Ongoing

BD ChloraPrep Scrub Teal

Reason Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

CareFusion 213, LLC NDC 54365-400-39 D-0650-2026