US Drug Recall Register
Class I · High risk Terminated Initiated Aug 22, 2022 (4 years ago)

PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop…

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

Why it was recalled

Presence of particulate matter

What was recalled

PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0409-4699-54) further packaged in a tray of 10 vials (NDC Carton: 0409-4699-24), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA

Recalling firm
Pfizer Inc.
NDC code
0409-4699-54
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1540-2022

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.

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