The Recall Desk
HighFDA (Devices)·Z-2848-2026·Announced 2026-08-12

Quantum Rehab Q6 Edge 2.0 Wheelchair Recall Due to Safety Risks

The FDA is recalling the Quantum Rehab Q6 Edge 2.0 powered wheelchair because its controller may cause unexpected braking or system crashes that could lead to falls and injuries.

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: The recall involves a Class II medical device with potential for serious injury (falls, control failures) where no injuries have been reported yet, matching the rubric criterion for High severity (risk-of-harm products where injury has not yet been reported).

Plain-English summary

The FDA is recalling the Quantum Rehab Q6 Edge 2.0 powered wheelchair because its controller may trigger unexpected park brake stops while driving or cause the control system to crash, both of which could lead to falls and injuries. This affects all owners of the Q6 Edge 2.0 (ilevel) model manufactured by Pride Mobility Products Corp., distributed worldwide including the United States. Consumers should stop using the device immediately and contact their dealer or the manufacturer for replacement or repair guidance.

The recalled product

Product
Brand Name: Quantum Rehab Product Name: Q6 Edge 2.0 (ilevel) Model/Catalog Number: Q6 Edge 2.0 (ilevel) 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 — Mobility Device
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 (ilevel) 0060650920004*2 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 →

Related recalls

Same manufacturer · Pride Mobility Products Corp.

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Same hazard · brake failure

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