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Baxter Healthcare Corporation 2024-12-04 Health serious FDA
Health · FDA · Recall #FDA-Z-0559-2025

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use… Recall

Issued December 4, 2024 · Baxter Healthcare Corporation

In December 2024, Baxter Healthcare Corporation recalled the Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use…, 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 has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

What you should do

  1. 1 Stop using Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use… 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
December 4, 2024
Units affected
Not reported
Sold at
Worldwide distribution.
Recall number
FDA-Z-0559-2025
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 737th Health recall we've logged in 2024.
Read the official FDA notice

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