Baxter Pro+ MRS Surfaces for VersaCare
PRO+ MRS Surface for Versacare has an error in its UDI label that may lead to incorrect product identification.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Baxter Healthcare Corporation of Deerfield, Illinois is recalling Pro+ MRS Surface for VersaCare, PRO+ 36" MRS Surface, and PRO+ 40" MRS Surface mattresses with Advanced Microclimate Technology because of an error in the product description on the Unique Device Identification label.
The labeling discrepancies do not align with the approved product or specifications and may lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame. The recall began August 18, 2026, and distribution was worldwide, including the US Nationwide and Canada.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your mattress affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
Product details
PRO+ MRS SURFACE FOR VERSACARE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/
- UDI-DI
- 00887761007543
- Catalog code
- P3255A08
Product details
PRO+ 40" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/
- UDI-DI
- 00887761007666
- Catalog code
- P7924A14
Product details
PRO+ 36" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and output valves to provide weight-based pressure redistribution whenever a patient moves or is repositioned, Model/
- UDI-DI
- 00887761007659
- Catalog code
- P7924A13
Details
- Company began the recall
- Sold in
Worldwide distribution - US Nationwide and the country of Canada.
- Event ID
- 99606
- Recall numbers
- Z-3262-2026 to Z-3264-2026
- Company
- Baxter Healthcare CorporationDeerfield, Illinois
- Hazard
- Labeling error
- Recall type
- Voluntary: Firm initiated
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
