Use cautionMedical device recall · FDA · Published June 25, 2026
Quantum Rehab R-TRAK Wheelchair Software 2.0.11 May Cause Unexpected Stops During Use
Quantum Rehab recalls R-TRAK wheelchair software version 2.0.11 due to potential unexpected stops when driving, which could cause falls or injuries. Affected units may need software update to 2.0.13.
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.
“Quantum Rehab R-TRAK Wheelchair Software 2.0.11 May Cause Unexpected Stops During Use.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/314314-quantum-rehab-r-trak-wheelchair-software-2-0-11-may. Based on FDA recall #Z-2844-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2844-2026%22&limit=1).
Pride Mobility Products Corp. is recalling Quantum Rehab R-TRAK powered wheelchairs with software version 2.0.11 due to a hazard that may cause unexpected brake stops or system crashes, the FDA said on June 25, 2026.
How to tell if you have it
Brand: Quantum Rehab
Product Name: R-TRAK
Model/Catalog Number: R-TRAK
Software Version: 2.0.11
Lot Code: R-TRAK 0060650920022*6 K011993 D049085 41875 ITI
The hazard
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 may perform an unexpected park brake stop, which may result in fall or injury. If not driving, the control system may crash and remain in pre-operational mode.
Context
GovInfoNow's records show Quantum Rehab has been subject to other recent recalls of similar products including Munevo Powered Wheelchair Hands-Free Control Software Issue May Cause Steering Drift (2026-06-19).
How to tell if you have this one
Check for Quantum Rehab R-TRAK wheelchairs with software version 2.0.11. The product description includes model number R-TRAK and lot code R-TRAK 0060650920022*6.
Brand
Quantum Rehab
Category
Medical device
FDA recall event · 13 products
All 13 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
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.
Install software version 2.0.13 to fix the issue. This update is available through Quantum Rehab.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 48 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA 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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 48 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2844-2026 (June 25, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2844-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.