RECALL DATABASE

Pride Mobility Products Corp. Q6 Edge 3 Stretto Recall

Announced 2026-08-12 · FDA

Pride Mobility is recalling 1,102 units of the Brand Name: Quantum Rehab Q6 Edge 3 Stretto wheelchair due to Remind Me Later reminders that may appear during use. If the reminder appears while driving, the wheelchair may perform an unexpected park brake stop, potentially causing a fall or injury; if it occurs while not driving, the control system may crash and remain in pre-operational mode. The recall covers worldwide distribution, including the United States, Canada, and Australia.

BrandPride Mobility Products Corp.
ProductBrand Name: Quantum Rehab Product Name: Q6 Edge 3 Model/Catalog Number: Q6 Edge 3 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
ReasonIf 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.
Severitymoderate
Units affected1102
DistributionWorldwide - 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.
AgencyFDA
Recall / campaign no.Lot Code: Q6 Edge 3 0060650920015*8 K143383 D246699 41875 ITI

WHAT YOU SHOULD DO

  1. Stop using the wheelchair immediately if a Remind Me Later reminder pops up while you are driving; safely bring the wheelchair to a stop.
  2. Contact Pride Mobility customer service or your authorized dealer to report the recall and arrange for inspection, repair, or a software update; provide the recall number Lot Code: Q6 Edge 3 0060650920015*8 K143383 D246699 41875 ITI.
  3. Do not attempt to repair or modify the wheelchair yourself; follow the official repair instructions provided by Pride Mobility or FDA.
  4. Monitor for additional recall updates from the FDA and Pride Mobility and install any approved software updates when advised.

This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.