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Class I: serious health riskTerminated

Pfizer PROPOFOL Injectable Emulsion Recall

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

Pfizer Inc. · New York, NY

Risk level
Class I
Reported by FDA
Sep 21, 2022
Recall ID
D-1540-2022
Check your lot numberHow we source this data

Summary

Pfizer recalled PROPOFOL Injectable Emulsion starting Aug 22, 2022. The FDA classified it as Class I (serious health risk) and published enforcement report D-1540-2022 on Sep 21, 2022. Reason: Presence of particulate matter. Status: Terminated.

Why it was recalled

Presence of particulate matter

Product description

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

Lot numbers, UPCs & expiration codes

Lot#: EA7470, Exp 6/1/2023

Where it was sold

USA Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1540-2022
Classification
Class I
Status
Terminated
Recall initiated
Aug 22, 2022
FDA report date
Sep 21, 2022
Quantity
5,390 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Pfizer Inc.

Original FDA data

Every field from FDA enforcement report D-1540-2022, exactly as published.

Show all FDA fields
City
New York
State
NY
Status
Terminated
Country
United States
Event ID
90785
Address
235 East 42nd Street
Code information
Lot#: EA7470, Exp 6/1/2023
Postal code
10017-5703
Report date
Sep 21, 2022
Product type
Drugs
Recall number
D-1540-2022
Classification
Class I
Recalling firm
Pfizer Inc.
Product quantity
5,390 vials
Termination date
Jun 30, 2025
Reason for recall
Presence of particulate matter
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
USA Nationwide
Recall initiation date
Aug 22, 2022
Initial firm notification
Press Release
Center classification date
Sep 19, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1540-2022, published Sep 21, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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