FDA Device recall Z-1882-2017
The Savaria Stairfriend is a Residential, commercial, indoor, stair lift for curved stairs
- FDA Device
- Class II
- terminated
- Published 2017-05-03
On 2017-05-03 the FDA classified a Class II recall of The Savaria Stairfriend is a Residential, commercial, indoor, stair lift for curved stairs by Savaria Concord Lifts, citing savaria Concord Lifts has decided to initiate a recall of the Stairfriend, because of product defect. The product defect relates to poor quality of welding holding the seat post .
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1882-2017 |
| 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
The Savaria Stairfriend is a Residential, commercial, indoor, stair lift for curved stairs.
Reason
Savaria Concord Lifts has decided to initiate a recall of the Stairfriend, because of product defect. The product defect relates to poor quality of welding holding the seat post .
Identifiers
| code_info | s/n or lot number - 690009 thru 690235 |
|---|
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-1882-2017%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.