Baxter Healthcare Corporation recalls PRO+ MRS SURFACE FOR VERSACARE
- Recalling company
- Baxter Healthcare Corporation
- Product
- 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/Catalog Number: P3255A08
- Reason
- There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product specifications and may lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 18, 2026
- Reported
- Sep 30, 2026
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Status
- Ongoing
- Quantity
- 169 units
- Lot / codes
- Serial Number: A171BP3769 - B057BP6765 UDI-DI Number: 00887761007543
- Company location
- Deerfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3262-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3262-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.