Progressa Bed — Class II medical device recall Z-1319-2018
Terminated recall by Hill-Rom, Inc., reported 2018-04-18, distributed nationwide. A component used within the braking system may break resulting in one or more brake pedals on the bed staying
| Recall number | Z-1319-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hill-Rom, Inc., Batesville, IN, United States |
| Recall initiated | 2018-01-12 |
| Classified | 2018-04-09 |
| Reported by FDA | 2018-04-18 |
| Terminated | 2020-06-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA, CL, CO, CR, ES, FR, GB, HK, IL, JM, JO, JP, MX, MY, OM, PA, SA, SG, TW |
| Quantity | 2,117 |
| Reason classes | device malfunction |
Product
Progressa Bed - AC-powered adjustable hospital bed
Reason for recall
A component used within the braking system may break resulting in one or more brake pedals on the bed staying in brake or not being engaged which could result in unwanted bed movement and possible 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-1319-2018. 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.