TemporaryFDAOngoing
Can cause harm that is usually temporary.
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/Catalog Number: P7924A13
Check the device or its packaging for
Serial Number: A136BP2433 - B052BP6510 UDI-DI Number: 00887761007659
- Why
- 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.
- Distributed
- Worldwide distribution - US Nationwide and the country of Canada.
- Company
- Baxter Healthcare Corporation
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-3263-2026 · retrieved 24 September 2026
Read the official notice