Hospira has voluntarily recalled 1 lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol) due to a visible particulate observed in a single vial.

Propofol is an intravenous general anesthetic and sedative drug for use in the induction and maintenance of anesthesia or sedation. The recalled lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol), 1g/100mL single patient use glass fliptop vial; NDC (vial) 0409-4699-54; NDC (carton) 0409-4699-24; Lot # DX9067; Expiration Date May 1, 2023, was distributed nationwide to wholesalers, hospitals, and the Department of Defense in the United States between June 10, 2020 and June 26, 2020.

To date, the Company has not received any adverse event reports related to this recall. Patients receiving the affected product may be at risk of life-threatening adverse events (eg, blockage of blood vessels); hypersensitivity reactions and infectious disease transmission may also be possible.

Adverse reactions or quality problems should be reported to the Food and Drug Administration’s MedWatch program.


Hospira issues a voluntary nationwide recall for one lot of Propofol Injectable Emulsion, USP (containing benzyl alcohol), due to the potential presence of visible particulate. News release. Hospira Inc. July 13, 2022. Accessed July 14, 2022. https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hospira-issues-voluntary-nationwide-recall-one-lot-propofol-injectable-emulsion-usp-containing