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Serious recall: Injury is possible or has been reported. Take action promptly.

Pfizer Inc. 2023-01-11 Health serious FDA
Health · FDA · Recall #FDA-D-0097-2023

Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride… Recall

Issued January 11, 2023 · Pfizer Inc.

In January 2023, Pfizer Inc. recalled the Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Lack of assurance of sterility: Bags have the potential to leak.

What you should do

  1. 1 Stop using Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Pfizer Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Pfizer Inc.
Category
Health
Recall date
January 11, 2023
Units affected
Not reported
Sold at
Nationwide in the USA.
Recall number
FDA-D-0097-2023
Made in
United States
Issuing agency
FDA

In context

  • Pfizer Inc. has 13 recalls in our database, including 5 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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