RegWardenFDA facility compliance records
Facility

Pride Mobility Products Corporation

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

Activity by year

FDA actions on record by year2010: 1 recalls; 2016: 1 recalls; 2026: 1 recalls1’10’11’12’13’14’151’16’17’18’19’20’21’22’23’24’251’26
  • Recalls (3)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2026-06-25
    If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this o…
  • Class IITerminated2016-12-01
    The interface between the TB3 back and tilt base can separate when tilted beyond the specified angle.
  • Class IITerminated2010-11-26
    The main harness connector was manufactured without the required back shield sealing protection. As a result, there is the potential for water to seep through the nonconforming harness.

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. “Pride Mobility Products Corporation (FEI 3044470904) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3044470904-pride-mobility-products-corporation/

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