- Recalling firm
- Pride Mobility Products Corp.
- 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.
- Affected products (lot / model / serial)
- Lot Code: Quantum 4Front 2HD 0060650920020*2 K143383 D246699 41875 ITI
- Units affected
- 1102
- Distribution pattern
- 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.
- Firm location
- Duryea, PA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2851-2026
- Recall initiated
- June 25, 2026
- FDA classification date
- July 31, 2026
- FDA report date
- August 12, 2026
- FDA event ID
- 99286
- Last updated on HTM Vibe
- August 18, 2026