The Recall Desk
HighFDA (Devices)·Z-2846-2026·Announced 2026-08-12

Quantum Rehab Q6 Edge 2.0 Power Wheelchair Recall

Pride Mobility is recalling 1,102 Q6 Edge 2.0 power wheelchairs due to a software issue that may cause unexpected braking or control system crashes during use.

What this means for you

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: This is an FDA Class II recall involving a risk-of-harm product where injury has not yet been reported, meeting the rubric criterion for High severity.

Plain-English summary

Pride Mobility Products Corp. is recalling 1,102 units of the Quantum Rehab Q6 Edge 2.0 power wheelchair. The recall involves wheelchairs with software version 2.0.11, which is being updated to version 2.0.13.

The issue stems from the user reminder feature. 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.

The recalled wheelchairs were distributed nationwide in the United States, including in numerous states, as well as in Canada and Australia. The lot code is Q6 Edge 2.0 0060650920004*2 K042612 D049086 41875 ITI.

Consumers should contact Pride Mobility Products Corp. to schedule a free software update. Until the update is performed, users should avoid selecting the 'Remind Me Later' option for user reminders.

The recalled product

Product
Brand Name: Quantum rehab Product Name: Q6 Edge 2.0 Model/Catalog Number: Q6 Edge 2.0 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 2.0 0060650920004*2 K042612 D049086 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 →

Related recalls

Same manufacturer · Pride Mobility Products Corp.

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Same hazard · fall injury

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