FDA Device recall Z-0728-2017
Carry bar which is an accessory to a lift used for patients in hospitals and other facilities
- FDA Device
- Class II
- terminated
- Published 2016-12-21
On 2016-12-21 the FDA classified a Class II recall of Carry bar which is an accessory to a lift used for patients in hospitals and other facilities by Ergosafe Products Dba Prism Medical, citing the black plastic puck on the carry bar is breaking resulting in potential for patient harm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0728-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-08-30 |
| Published | 2016-12-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ergosafe Products Dba Prism Medical |
| Distribution | US |
Product
Carry bar which is an accessory to a lift used for patients in hospitals and other facilities. Recall impacts the following model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757.
Reason
The black plastic puck on the carry bar is breaking resulting in potential for patient harm.
Identifiers
| code_info | There are no lot numbers, serial numbers, or UPC codes, only the model numbers. Model numbers: 360741, 360750, 36075…There are no lot numbers, serial numbers, or UPC codes, only the model numbers. Model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757. |
|---|
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-0728-2017%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.