# FDA recall Z-1130-2022

> **Invacare Corporation** · Class II · device recall initiated 2022-03-30.

## 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.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AK, AR, CA, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NY, OH, OR, PA, SC, TN, TX, VA, VT, WA, and WI. The country of Canada.

## Key facts

- **Recall number:** Z-1130-2022
- **Recalling firm:** Invacare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-03-30
- **Report date:** 2022-06-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Elyria, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1130-2022

## Citation

> AI Analytics. FDA recall Z-1130-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1130-2022. Source: US FDA. Licensed CC0.

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