Facility

PRIDE MOBILITY PRODUCTS CORP.

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

Key facts

3recalls · worst Class II

2inspections · worst NAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3007608806
Establishment type	Manufacture Medical Device
Location	3200 E Gowan Road North Las Vegas, NV, US 89030
Registration status	Active · expires 2026
Parent company	PRIDE MOBILITY PRODUCTS CORP. (owner-operator 2523375)
Brand names	BELT, WHEELCHAIR

Activity by year

Recalls (3)
Inspections (2)

Devices registered here (1)

Belt, Wheelchair
Product code IQB (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3920

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.

FDA inspections (2)

NAI2019-12-04
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
NAI2016-07-25
No Action Indicated · Compliance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

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 CORP. (FEI 3007608806) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007608806-pride-mobility-products-corp/

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