Data Foundry

Medical device recalls 2015

Storm Series Electric Wheelchair — Class II medical device recall Z-1139-2015

Terminated recall by Invacare Corporation, reported 2015-03-04, distributed nationwide. If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight

Recall numberZ-1139-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmInvacare Corporation, Elyria, OH, United States
Recall initiated2015-01-15
Classified2015-02-20
Reported by FDA2015-03-04
Terminated2015-09-23
DistributedNationwide (US)
Countries outside the USAU, CA
Quantity525
Model numbers06GE005314, 06IE008666, 06JE005407, 06JE005408, 06JE006242, 06JE007067, 06KE002230, 06KE006044, 06LE000137, 06LE003960, 06LE005870, 06LE005873, 06LE005998, 06LE007409, 07AE000992, 07BD001779, 07BE001559, 07BE001777, 07BE001779, 07BE003307, 07BE004040, 07BE005320, 07BR003307, 07CE003237, 07CE004842 and 475 more

Product

Storm Series Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width configurations with power recline seating system and a conventional style back.

Reason for recall

If the slack in the wires is not routed and secured correctly, flexing of the back pan under the users weight may cause the headrest knob or clamp bracket to pinch, damage or cut the wire. Smoking, sparking, burning or fire may occur if a wire is repetitively pinched at the same place.

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-1139-2015. 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.