# FDA recall Z-1415-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-06-24.

## Product

Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.

## Reason for recall

The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, CT, GA, IA, IN, KY, LA, MD, MI, MN, MO, NC, NJ, NM, NM, NY, OH, OK, RI, SD, TN, TX, VT, and WI.  There was government distribution but no military distribution. The country of Canada.

## Key facts

- **Recall number:** Z-1415-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-24
- **Report date:** 2022-07-27

- **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-1415-2022

## Citation

> AI Analytics. FDA recall Z-1415-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1415-2022. Source: US FDA. Licensed CC0.

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