Omega Incline Platform Lift — Class II medical device recall Z-1880-2017
Terminated recall by Savaria Concord Lifts, Inc., reported 2017-05-03. Savaria Concord Lifts Inc has decided to initiate this recall of its Omega Incline Platform Lift because bolts
| Recall number | Z-1880-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Savaria Concord Lifts, Inc., Brampton, N/A, Canada |
| Recall initiated | 2017-04-12 |
| Classified | 2017-04-26 |
| Reported by FDA | 2017-05-03 |
| Terminated | 2017-10-16 |
| Quantity | 74 |
| Lot numbers | 630046 |
Product
Omega Incline Platform Lift
Reason for recall
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
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-1880-2017. 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.