ProductGuru Recalls

Official recall record

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

US FDA — Medical Devices · 2024-03-05 · United StatesClass II
Issuing authority
US FDA — Medical Devices
Alert date
2024-03-05
Country of alert
United States
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
00887761977884
Brand on record
Baxter Healthcare Corporation

What the authority reported

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

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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