Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/Catalog Number: Q6 Edge 3 So…

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 occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

Firm notified dealers and consumers via mailed letters on June 25, 2026. Dealers were instructed to locate affected units and inform consumers of the required software update. Dealers should schedule service appointments with affected consumers. Systems should be updated to Q-Logic software version 2.0.13 or later. The update must be completed following a system power cycle. Consumers were instructed to disable the "Remind Me Later" feature immediately. Consumers should contact their dealer to schedule an appointment for software update.

• FDA enforcement recordOfficial FDA database entry for Z-2849-2026
• FDA 510(k) clearance · K143383The device's official FDA premarket clearance record
• FDA device classification · ITIOfficial FDA classification for this device type
• CFR regulation · 21 CFR 890.3860The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Pride Mobility Products Corp.Search for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.