Baxter Healthcare Corporation 2025-12-10 Health serious FDA
Health · FDA · Recall #FDA-Z-0847-2026
Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product … Recall
Issued December 10, 2025 · Baxter Healthcare Corporation
In December 2025, Baxter Healthcare Corporation recalled the Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product …, 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
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the replacement kits.
What you should do
- 1 Stop using Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Baxter Healthcare Corporation to arrange your voluntary. See the official notice below for contact details.
- 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 10, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of California, Colorado, Ohio, and Utah.
- Recall number
- FDA-Z-0847-2026
- 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 691st Health recall we've logged in 2025.