FDA Device recall Z-1130-2022
Invacare TDX SP2, Model Nos
- FDA Device
- Class II
- ongoing
- Published 2022-06-01
On 2022-06-01 the FDA classified a Class II recall of Invacare TDX SP2, Model Nos by Invacare, citing the battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1130-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-03-30 |
| Published | 2022-06-01 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Invacare |
| Distribution | US |
Product
Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
Reason
The battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or impact to the wheelchair. The disconnection of the battery harness results in loss of power to the wheelchair.
Identifiers
| code_info | UDI (DI): Model Number Device Identifier TDXSP2 00841447100911 TDXSP2-MCG 00841447100966 TDXSP2V 0084144…UDI (DI): Model Number Device Identifier TDXSP2 00841447100911 TDXSP2-MCG 00841447100966 TDXSP2V 00841447101512 Serial Numbers: 22CE000031 22BE004288 22BE002669 22BE003672 22BE004782 22BE004151 22CE000984 22BE004286 22BE004171 22BE004540 22CE001086 22BE003661 22CE000184 22CE000878 22CE001449 22CE000032 22CE001421 22BE004933 22CE001002 22CE000180 22CE000725 22BE004544 22BE005009 22BE003671 22BE004284 22BE004159 22BE004285 22BE002652 22BE004282 22BE004798 22BE004281 22BE004170 22CE000182 22CE000183 22CE000876 22CE000873 22CE000981 22CE000870 22CE000871 22CE001248 22CE001004 22CE001084 22BE004776 22BE004165 22BE004931 22BE005010 22CE000875 22CE000728 22CE000727 22BE004910 22BE004904 22BE005007 22BE004160 22BE004169 22BE004175 22BE004166 22BE004905 22CE001420 22CE000496 22BE003645 22BE002651 22CE000999 22CE001078 22BE004545 22BE004763 22BE003662 22BE004929 22BE004937 22BE004176 22BE004903 22CE000181 22BE004167 22BE005006 22BE002666 22BE004177 22BE003962 22BE003957 22BE0041 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1130-2022%22
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