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Recall Observatory FDA recall evidence

Drug product

Propofol Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL per 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

D-1301-2022

July 13, 2022

Class I

Product summary

Firm
Pfizer Inc.
Event
Event 90581
Status
Terminated
Classification
Class I
Quantity
54,000 vials
Official record key
drug-enforcement:D-1301-2022

Official wording

Reason: Presence of particulate matter: particulate identified as a beetle.

Code information: Lot #: DX9067, Exp 5/1/2023

Distribution pattern: USA Nationwide

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    particulate matter