Invacare TDX SP2 — Class II medical device recall Z-1130-2022
Ongoing recall by Invacare Corporation, reported 2022-06-01, distributed nationwide. The battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or
| Recall number | Z-1130-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Invacare Corporation, Elyria, OH, United States |
| Recall initiated | 2022-03-30 |
| Classified | 2022-05-25 |
| Reported by FDA | 2022-06-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 133 devices |
| UPC / GTIN / UDI-DI | 00841447100911, 00841447100966, 00841447101512 |
| Serial numbers | 22BE002651, 22BE002652, 22BE002666, 22BE002669, 22BE002932, 22BE002934, 22BE002935, 22BE002936, 22BE003645, 22BE003659, 22BE003661, 22BE003662, 22BE003664, 22BE003671, 22BE003672, 22BE003673, 22BE003957, 22BE003959, 22BE003960, 22BE003961, 22BE003962, 22BE003963, 22BE004151, 22BE004159, 22BE004160 and 108 more |
| Model numbers | TDXSP2, TDXSP2-MCG, TDXSP2V |
Product
Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
Reason for recall
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.
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-1130-2022. 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.