FDAMarch 5, 2024device

Hill-Rom PRO+ 36" MRS Surface, REF P7924A03, The pro+ mattress is intended for patient support and for the prevention and/or treatment of pressure injuries.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Inconsistencies were identified with service records associated with corrections performed for a previous Medical Device Correction issued by Baxter (ref number: FA-2022-026). Your devices have been identified as potentially impacted by these service inconsistencies and therefore, Baxter will need to reassess the impacted mattresses to confirm they have been corrected as identified by the service order, and to confirm the correct serial numbers have been identified.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

00887761977884

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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