RegWardenFDA facility compliance records
Facility

TISPORT, LLC

2 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2018: 1 recalls; 2021: 1 recalls201712018201920201202120222023202420252026
  • Recalls (2)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2021-09-24
    Some affected wheelchairs, with transit tie downs, that are used as a passenger seat in a motor vehicle may not be configured in the right orientation to perform as intended if involved in a motor vehicle accident. Some affected wheelchairs can no longer be used as a passenger se…
  • Class IITerminated2018-09-11
    The anti-tip tubes potentially fail in certain situations and the wheelchairs can tip backwards.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “TISPORT, LLC (FEI 3002653226) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002653226-tisport-llc/

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