# FDA recall Z-1400-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2024-03-05.

## Product

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.

## Reason for recall

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.

## Distribution

US Nationwide distribution in the state of Colorado.

## Key facts

- **Recall number:** Z-1400-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-05
- **Report date:** 2024-04-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1400-2024

## Citation

> AI Analytics. FDA recall Z-1400-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1400-2024. Source: US FDA. Licensed CC0.

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