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.
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 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
- 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
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.
See all →- SevereQuantum Rehab Q6 Edge 4 Wheelchairs Recalled Due to Controller Software Issue
FDA (Devices) · 2026-08-12
- HighQuantum Rehab Q6 Edge 2.0 Power Wheelchair Recall
FDA (Devices) · 2026-08-12
- HighQuantum 4Front 2HD Powered Wheelchair Recall Due to Potential Safety Issues
FDA (Devices) · 2026-08-12
- HighQuantum Rival Powered Wheelchair Controller Recall for Brake Stop Hazard
FDA (Devices) · 2026-08-12
- SeverePowered Wheelchair Controller Software Recall by Pride Mobility
FDA (Devices) · 2026-08-12
Same hazard · brake failure
See all →- Severe
- Severe
- SevereNova Bus Recalls 2024-2025 LFS Transit Buses for Parking Brake Defect
NHTSA · 2026-09-22
- Severe
- SeverePeterbilt Recalls 2027 548 Trucks Due to Brake Valve Size Issues
NHTSA · 2026-09-01
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