Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
Reported: June 1, 2022 Initiated: March 30, 2022 #Z-1130-2022
Product Description
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.
Details
- Recalling Firm
- Invacare Corporation
- Units Affected
- 133 devices
- 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.
- Location
- Elyria, OH
Frequently Asked Questions
What product was recalled? ▼
Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V. Recalled by Invacare Corporation. Units affected: 133 devices.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 1, 2022. Severity: Moderate. Recall number: Z-1130-2022.
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