FDA Device recall Z-1405-2017
A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124
- FDA Device
- Class II
- terminated
- Published 2017-03-15
On 2017-03-15 the FDA classified a Class II recall of A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124 by Ergosafe Products Dba Prism Medical, citing during internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1405-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-01-30 |
| Published | 2017-03-15 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ergosafe Products Dba Prism Medical |
| Distribution | MT, NV, VA |
Product
A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
Reason
During internal cycle test at max load (625 lbs.) 2 units had straps break prematurely.
Identifiers
| code_info | A6MC000110 A6M0001010 A6M0001011 A6M0001012 A6M0001013 A6M0001014 A6M0001015 A6M0001016 A6M0001017 A6M0001018…A6MC000110 A6M0001010 A6M0001011 A6M0001012 A6M0001013 A6M0001014 A6M0001015 A6M0001016 A6M0001017 A6M0001018 A6M0001019 A6M0001020 A6M0001021 A6M0001025 A6M0001026 A6M0001029 A6M0001022 A6M0001023 A6M0001024 A6M0001027 A6M0001028 |
|---|
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-1405-2017%22
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