Quantum Rehab R-TRAK Powered Wheelchair Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Pride Mobility Products Corp. is recalling 1,102 Quantum Rehab R-TRAK controllers (software version 2.0.11) due to potential unexpected park brake stops or system crashes.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 19, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
Pride Mobility Products Corp. initiated a voluntary recall after determining that selecting the "Remind Me Later" option for user reminders may cause pop-up messages to appear while the wheelchair is in use. This can result in an unexpected park brake stop while driving, potentially leading to a fall or injury, or a control system crash if not driving.
Which Products Are Affected
The recall involves the Quantum Rehab R-TRAK powered wheelchair controller, model/catalog number R-TRAK, software version 2.0.11 (new version 2.0.13). Product description: Wheelchair, Powered (ITI), 890.3860, Component: Controller. A total of 1,102 units are affected. Lot code: R-TRAK 0060650920022*6 K011993 D049085 41875 ITI. Distribution is nationwide across the United States (including 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) as well as Canada and Australia.
What You Should Do
The recall was initiated voluntarily by the firm via letter. Consumers should refer to the recall notice for further guidance on the affected devices.
Why This Matters
The Class II recall addresses a software issue that may cause unexpected stops or system crashes in powered wheelchairs, posing a risk of falls or injuries during use.
Source
U.S. Food and Drug Administration, recall number Z-2844-2026, event ID 99286.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,476 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 19, 2026.
Frequently Asked Questions
Common questions about this FDA recall.