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FDA (Device enforcement)Recalled 2026-08-18class ii

Baxter Healthcare Corporation: 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 pressu

Is my product affected?

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

  • UPC 00887761007543

Check against the official notice below — it lists the full affected range.

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: Worldwide distribution - US Nationwide and the country of Canada. Quantity: 169 units Lot/code info: Serial Number: A171BP3769 - B057BP6765 UDI-DI Number: 00887761007543

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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