Reported Jun 1, 2022 · Ongoing

Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V

Invacare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Invacare Corporation · 1200 Taylor St · Elyria, OH · 44035-6248

Is this the product you have?

    • Invacare TDX SP2
    • Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V
Lot codes and dates
  • UDI (DI)Model Number Device Identifier TDXSP2 00841447100911 TDXSP2-MCG 00841447100966
  • TDXSP2V 00841447101512 Serial Numbers

    133 of 133 codes

    • 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
Amount recalled
133 devices

Where it was sold

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Invacare Corporation recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.