Drug recall D-1540-2022
Product
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
Reason for recall
Presence of particulate matter
Lots and codes
Lot#: EA7470, Exp 6/1/2023
Recall details
- Recalling firm
- Pfizer Inc., New York, NY
- Quantity
- 5,390 vials
- Distribution
- USA Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 22, 2022
- Terminated
- June 30, 2025
Related products
- Propofol – drug information
- NDC 0409-0010 Propofol · Propofol 10 mg/mL · Hospira, Inc.
- NDC 0409-4699 Propofol · Propofol 10 mg/mL · Hospira, Inc.
- NDC 0409-0501 Propofol · Propofol 10 mg/mL · Hospira, Inc.
- NDC 0409-6010 Propofol · Propofol 10 mg/mL · Hospira, Inc.
- NDC 0409-1511 Propofol · Propofol 10 mg/mL · Hospira, Inc.