Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2091-2014 — MK5 NX Controller--Wheelchair controller

U.S. FDA — Device Enforcement · United States · 2014-06-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2091-2014
Date of alert
2014-06-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Invacare Corporation
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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