RegWardenFDA facility compliance records
Company

PRIDE MOBILITY PRODUCTS CORP.

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

Recalls 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)

Registered facilities (6)

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.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “PRIDE MOBILITY PRODUCTS CORP. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-2523375-pride-mobility-products-corp/

Not open yet

Alerts for PRIDE MOBILITY PRODUCTS CORP.

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.