Recall Z-2846-2026

Pride Mobility Products Corp. · initiated June 25, 2026

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

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

Codes / lots: Lot Code: Q6 Edge 2.0 0060650920004*2 K042612 D049086 41875 ITI

Reason for recall

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.

FDA-determined cause: Under Investigation by firm

Action taken

Firm notified dealers and consumers via mailed letters on June 25, 2026. Dealers were instructed to locate affected units and inform consumers of the required software update. Dealers should schedule service appointments with affected consumers. Systems should be updated to Q-Logic software version 2.0.13 or later. The update must be completed following a system power cycle. Consumers were instructed to disable the "Remind Me Later" feature immediately. Consumers should contact their dealer to schedule an appointment for software update.

Details

Recall number
Z-2846-2026
Initiated
June 25, 2026
Posted by FDA
July 31, 2026
Product code
ITI – Wheelchair, Powered
Quantity
1102
Distribution
Worldwide - US Nationwide distribution including in the states of AZ, NJ, PA, OK, CO, IN, AR, KS, CT, MD, WI, TX, FL, WA, NY, MO, LA, UT, OR, VA, RI, CA, TN, MN, KY, NV, GA, WV, IL, OH, SC, WY, AL, MI, ME, NC, SD, DE, MA, NE, ND, IA, NH, NM, MT, ID, MS, DC, AK and the countries of Canada and Australia.
Recalling firm
Pride Mobility Products Corp., Duryea, PA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2841-2026 Class IIBrand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum…If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while… 06/25/2026Open, Classified
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Z-2844-2026 Class IIBrand Name: Quantum Rehab Product Name: R-TRAK Model/Catalog Number: R-TRAK Software…If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while… 06/25/2026Open, Classified
Z-2845-2026 Class IIBrand Name: Quantum Rehab Product Name: Q6 Edge HD Model/Catalog Number: Q6 Edge HD…If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while… 06/25/2026Open, Classified
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Z-2849-2026 Class IIBrand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/Catalog Number: Q6 Edge 3…If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while… 06/25/2026Open, Classified
Z-2850-2026 Class IIBrand Name: Quantum Rehab Product Name: Q6 Edge 4 Model/Catalog Number: Q6 Edge 4…If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while… 06/25/2026Open, Classified
Z-2851-2026 Class IIBrand Name: Quantum Rehab Product Name: Quantum 4Front 2HD Model/Catalog Number: Quantum…If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while… 06/25/2026Open, Classified
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Z-2853-2026 Class IIBrand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum…If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while… 06/25/2026Open, Classified