FDA recall, , Moderate risk
Quantum Rehab Power Wheelchairs
Quantum Rehab powered wheelchairs may show reminder pop-ups while in use, which can cause an unexpected park brake stop and lead to a fall or injury.
Summary by Recall Canary from the FDA notice
What happened
Pride Mobility Products Corp., of Duryea, Pennsylvania, is recalling Quantum Rehab powered wheelchairs, including the Q6 Edge 3 Stretto, Quantum Outback, Quantum 4Front 2, 4Front, Q6 Edge HD, Quantum 1450, Quantum Rival, R-Trak, Q6 Edge 3, Q6 Edge 2.0, Q6 Edge 2.0 (ilevel), Q6 Edge 4, and Quantum 4Front 2HD, because 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 may perform an unexpected park brake stop, which may result in fall or injury. If it occurs while not driving, the control system may crash and remain in pre-operational mode.
The recall began June 25, 2026, and was added to the FDA's Enforcement Report on July 31, 2026. The wheelchairs were distributed nationwide in the United States, including in states such as Arizona, New Jersey, Pennsylvania, and Texas, and in Canada and Australia.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
13 products
Match the UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Quantum Rehab Q6 Edge 3 Stretto
- UDI-DI
- 0060650920018
- Lot code
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Quantum Outback
- UDI-DI
- 0060650920024
- Lot code
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Quantum 4Front 2
- UDI-DI
- 0060650920019
- Lot code
- 4Front
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab 4Front
- UDI-DI
- 0060650920003
- Lot code
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Q6 Edge HD
- UDI-DI
- 0060650920005
- Lot code
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Quantum 1450
- UDI-DI
- 0060650920009
- Lot code
- 1450
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Quantum Rival
- UDI-DI
- 0060650920013
- Lot code
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab R-TRAK
- UDI-DI
- 0060650920022
- Lot code
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Q6 Edge 3
- UDI-DI
- 0060650920015
- Lot code
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum rehab Q6 Edge 2.0
- UDI-DI
- 0060650920004
- Lot code
- 2.0
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Q6 Edge 2.0 (ilevel)
- UDI-DI
- 0060650920004
- Lot code
- 2.0
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Q6 Edge 4
- UDI-DI
- 0060650920028
- Lot code
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Quantum Rehab Quantum 4Front 2HD
- UDI-DI
- 0060650920020
- Lot code
- 4Front
- 2HD
- 41875
- Software version
- 2.0.11, new version: 2.0.13
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide distribution including in the states of Arizona, New Jersey, Pennsylvania, Oklahoma, Colorado, Indiana, Arkansas, Kansas, Connecticut, Maryland, Wisconsin, Texas, Florida, Washington, New York, Missouri, Louisiana, Utah, Oregon, Virginia, Rhode Island, California, Tennessee, Minnesota, Kentucky, Nevada, Georgia, West Virginia, Illinois, Ohio, South Carolina, Wyoming, Alabama, Michigan, Maine, North Carolina, South Dakota, Delaware, Massachusetts, Nebraska, North Dakota, Iowa, New Hampshire, New Mexico, Montana, Idaho, Mississippi, District of Columbia, Alaska and the countries of Canada and Australia.
- Company
- Pride Mobility Products Corp.Duryea, Pennsylvania
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99286
- Recall numbers
- Z-2841-2026 to Z-2853-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
