Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: Q6 Edge 4
- Recalling company
- Pride Mobility Products Corp.
- Product
- Brand Name: Quantum Rehab Product Name: Q6 Edge 4 Model/Catalog Number: Q6 Edge 4 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 25, 2026
- Reported
- Aug 12, 2026
- 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.
- Status
- Ongoing
- Quantity
- 1102
- Lot / codes
- Lot Code: Q6 Edge 4 0060650920028*8 K143383 D246699 41875 ITI
- Company location
- Duryea, PA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2850-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2850-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.