FDA Device recall Z-1880-2017
Omega Incline Platform Lift
- FDA Device
- Class II
- terminated
- Published 2017-05-03
On 2017-05-03 the FDA classified a Class II recall of Omega Incline Platform Lift by Savaria Concord Lifts, citing savaria Concord Lifts Inc has decided to initiate this recall of its Omega Incline Platform Lift because bolts can come loose causing the carriage to separate from the trolley and….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1880-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-12 |
| Published | 2017-05-03 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Savaria Concord Lifts |
| Distribution | n/a |
Product
Omega Incline Platform Lift
Reason
Savaria Concord Lifts Inc has decided to initiate this recall of its Omega Incline Platform Lift because bolts can come loose causing the carriage to separate from the trolley and the unit to fail
Identifiers
| code_info | s/n or lot number - Job Number 630046 through 630119 |
|---|
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-1880-2017%22
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