Fresh Recalls

PRO+ MRS SURFACE FOR VERSACARE: recall status

Notice names this product. Baxter Healthcare’s PRO+ MRS SURFACE FOR VERSACARE is named in FDA Class II recall Z-3262-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported 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. Identifying details: Serial Number: A171BP3769 - B057BP6765 UDI-DI Number: 00887761007543. Units affected: 169 units. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
PRO+ MRS SURFACE FOR VERSACARE
Company / brand
Baxter Healthcare
Lot / serial / date codes
Serial Number: A171BP3769 - B057BP6765 UDI-DI Number: 00887761007543
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand
Baxter Healthcare

Recalls naming this model

FDA Class II · Medical device · September 30, 2026

PRO+ MRS SURFACE FOR VERSACARE recall — Baxter Healthcare Corporation

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 spec…

Company / brand: Baxter Healthcare recalls

Affected product: PRO+ MRS SURFACE FOR VERSACARE recall status

Official ID Z-3262-2026 · Official record ↗

See all Baxter Healthcare recalls →

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 12:00 PM UTC.