# FDA recall Z-2737-2020

> **Hill-Rom, Inc.** · Class II · device recall initiated 2020-06-30.

## Product

Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Percussion/Vibration Therapy.

## Reason for recall

Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of this screw could result in serious patient or user injury.

## Distribution

Worldwide distribution - US nationwide distribution including in the states of AR, AZ, CA, DE, IN, KY, MD, ME, MI, MO, NC,   NM, NY, OH, OK, PA, SC, TN, TX, VA, WA, WI, WV and the country of Canada.

## Key facts

- **Recall number:** Z-2737-2020
- **Recalling firm:** Hill-Rom, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-30
- **Report date:** 2020-08-05
- **Termination date:** 2022-10-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Batesville, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2737-2020

## Citation

> AI Analytics. FDA recall Z-2737-2020. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2737-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*