Progressa Bed — Class II medical device recall Z-2737-2020
Terminated recall by Hill-Rom, Inc., reported 2020-08-05, distributed nationwide. Affected beds may have screws installed that do not meet material tensile strength requirements. Failure of th
| Recall number | Z-2737-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hill-Rom, Inc., Batesville, IN, United States |
| Recall initiated | 2020-06-30 |
| Classified | 2020-07-30 |
| Reported by FDA | 2020-08-05 |
| Terminated | 2022-10-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 257 |
| Reason classes | potency |
| Model numbers | P7500 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2737-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.