Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2853-2026Class II

Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum Rival Software Version...

Pride Mobility Products Corp / initiated 2026-06-25 / Open, Classified

Pride Mobility Products Corp. began a recall of Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum Rival Software Version: 2.0.11, new version: 2.0.13 Product Description... on . FDA classified it as Class II and gives the reason as "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...". As of , the recall status on record is Open, Classified.

Recall record

Recall number
Z-2853-2026
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
Pride Mobility Products Corp
Product
Brand Name: Quantum Rehab Product Name: Quantum Rival Model/Catalog Number: Quantum Rival Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Product code
ITI Wheelchair, Powered
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 root cause
Under Investigation by firm
Action
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.
Quantity in commerce
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.
Product codes and lots
Lot Code: Quantum Rival 0060650920013*4 K011993 D049085 41875 ITI

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2853-2026
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-2841-2026Class IIOngoingVoluntary: Firm initiated
Z-2842-2026Class IIOngoingVoluntary: Firm initiated
Z-2843-2026Class IIOngoingVoluntary: Firm initiated
Z-2844-2026Class IIOngoingVoluntary: Firm initiated
Z-2845-2026Class IIOngoingVoluntary: Firm initiated
Z-2846-2026Class IIOngoingVoluntary: Firm initiated
Z-2847-2026Class IIOngoingVoluntary: Firm initiated
Z-2848-2026Class IIOngoingVoluntary: Firm initiated
Z-2849-2026Class IIOngoingVoluntary: Firm initiated
Z-2850-2026Class IIOngoingVoluntary: Firm initiated
Z-2851-2026Class IIOngoingVoluntary: Firm initiated
Z-2852-2026Class IIOngoingVoluntary: Firm initiated
Z-2853-2026Class IIOngoingVoluntary: Firm initiated