# FDA recall Z-0231-2023

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-10-18.

## Product

Hill-Rom Progressa Bed System

## Reason for recall

The compression links on impacted Progressa beds, listed in Appendix A, may bend when raising the head section. The labeling for these beds list a maximum patient weight of 500 lbs., however the bending may still occur with a patient weight of less than 500 lbs. depending on the patient 's position on the bed.

## Distribution

Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, HI, IN, LA, MA, MO, NC, NM, NV, NY, OK, OR, PA, SC. TN, TX, WA, and WI.  (UPDATED:   States of PA and SC and there was government distribution.) There was no military distribution.  Foreign distribution was made to Canada, Qatar, Singapore, and UAE.  UPDATE:  Saudi Arabia now included.

## Key facts

- **Recall number:** Z-0231-2023
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-18
- **Report date:** 2022-11-23

- **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-0231-2023

## Citation

> AI Analytics. FDA recall Z-0231-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0231-2023. Source: US FDA. Licensed CC0.

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