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

Baxter Healthcare Corporation 2022-08-31 Health serious FDA
Health · FDA · Recall #FDA-Z-1578-2022

Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Dark Blue: a) 25 pack REF… Recall

Issued August 31, 2022 · Baxter Healthcare Corporation

In August 2022, Baxter Healthcare Corporation recalled the Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Dark Blue: a) 25 pack REF…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

There is a potential of the packaging not maintaining a sterile barrier for the tip caps.

What you should do

  1. 1 Stop using Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Dark Blue: a) 25 pack REF… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Baxter Healthcare Corporation 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
Baxter Healthcare Corporation
Category
Health
Recall date
August 31, 2022
Units affected
Not reported
Sold at
Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.
Recall number
FDA-Z-1578-2022
Made in
United States
Issuing agency
FDA

In context

  • Baxter Healthcare Corporation has 36 recalls in our database, including 5 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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