FDA Device recall Z-1632-2020
Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs
- FDA Device
- Class II
- terminated
- Published 2020-04-08
On 2020-04-08 the FDA classified a Class II recall of Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs by Merits Holdings, citing pinion gear may disengage from track allowing lift to slip or jolt.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1632-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-03-02 |
| Published | 2020-04-08 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Merits Holdings |
| Distribution | US |
Product
Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs.
Reason
Pinion gear may disengage from track allowing lift to slip or jolt.
Identifiers
| code_info | Model: E60424YLMUB; SN: MU180600588; (01) 04714379292589 (11)190604 (21) MU190600025. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1632-2020%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.