Quantum Q6 Edge 2.0 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 Q6 Edge 2.0 powered wheelchairs due to a software issue that may cause 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, Devices.
What Happened
Pride Mobility Products Corp. initiated a voluntary recall of certain powered wheelchairs 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 if 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 Q6 Edge 2.0 powered wheelchair (Model/Catalog Number: Q6 Edge 2.0, Software Version: 2.0.11, new version: 2.0.13). A total of 1,102 units are affected. Distribution was 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. Lot Code: Q6 Edge 2.0 0060650920004*2 K042612 D049086 41875 ITI. Recall number Z-2846-2026.
What You Should Do
Consumers should contact Pride Mobility Products Corp. for further instructions regarding the software update or other actions.
Why This Matters
The software defect may cause sudden stops or system issues during use, posing a risk of falls or injuries to users.
Source
FDA recall Z-2846-2026, 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 (1,346 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.