MK5 NX Controller--Wheelchair controller — Class II medical device recall Z-2091-2014
Terminated recall by Invacare Corporation, reported 2014-07-30, distributed nationwide. M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have controllers that were programmed in
| Recall number | Z-2091-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Invacare Corporation, Elyria, OH, United States |
| Recall initiated | 2014-06-24 |
| Classified | 2014-07-22 |
| Reported by FDA | 2014-07-30 |
| Terminated | 2014-10-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 819 |
Product
MK5 NX Controller--Wheelchair controller
Reason for recall
M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have controllers that were programmed in a way this is not aligned to standard factory settings. The controller during different settings such as max forward speed, max forward acceleration, max reverse speed and max turning speed can result in momentary loss of control.
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-2091-2014. 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.