The Recall Desk
Agency classClass IIOur severity:HighFDA (Devices)·Z-2849-2026·Announced 2026-08-12

Quantum Rehab Q6 Edge 3 Powered Wheelchair Controller Recalled for Unexpected Braking

Pride Mobility Products Corp. is recalling the Quantum Rehab Q6 Edge 3 powered wheelchair controller due to a software issue that can cause unexpected braking and potential injury.

The agency’s classification

FDA (Devices): Class II

Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 3/5 (High).

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a high-risk product where a software defect could cause unexpected braking and potential injury, though no injuries have been reported in the source text.

Plain-English summary

Pride Mobility Products Corp. is recalling the Quantum Rehab Q6 Edge 3 powered wheelchair (Model/Catalog Number: Q6 Edge 3) due to a software issue in the controller. The issue involves the 'Remind Me Later' option for user reminders.

If the 'Remind Me Later' option is selected, a reminder pop-up may appear while the wheelchair is in use. If this occurs while the wheelchair is being driven, it may perform an unexpected park brake stop, which could result in a fall or injury. If the pop-up appears while the wheelchair is not being driven, the control system may crash and remain in pre-operational mode.

This recall affects approximately 1,102 units distributed worldwide, including in the United States, Canada, and Australia. Affected units include software version 2.0.11; a new version, 2.0.13, is available.

The recalled product

Product
Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/Catalog Number: Q6 Edge 3 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Manufacturer
Pride Mobility Products Corp.
Category
Medical Device — Powered Wheelchair
Hazard
Affected units
1,102

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot Code: Q6 Edge 3 0060650920015*8 K143383 D246699 41875 ITI

Distribution

Distributed nationwide across the United States.

The notice also names 49 states specifically:

Part of a larger recall action

This product is one of 13 recalled by Pride Mobility Products Corp. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 13 products in this recall →

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