FDA Device recall Z-1319-2018
Progressa Bed - AC-powered adjustable hospital bed
- FDA Device
- Class II
- terminated
- Published 2018-04-18
On 2018-04-18 the FDA classified a Class II recall of Progressa Bed - AC-powered adjustable hospital bed by Hill Rom, citing 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 move….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1319-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-01-12 |
| Published | 2018-04-18 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Hill Rom |
| Distribution | US |
Product
Progressa Bed - AC-powered adjustable hospital bed
Reason
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.
Identifiers
| code_info | S159AW9192 through S305AW2321 Beds manufactured from June 8, 2017 to November 1, 2017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1319-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.