Quantum 1450 Quantum 1450 / Q1450Recalls & reported problems
Pride Mobility Products Corp · A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00606509200097), received between Jun 14, 2021 and Mar 19, 2026 — classified as 3 injuries.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available3
Patient problems
- Bone Fracture(s)2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Bruise/Contusion1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMar 19, 2026Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER ALLEGES CHAIR WAS TILTED BACK AND HEARD A POP AND BACK GAVE WAY ALLEGEDLY CAUSING THE CHAIR TO FLIP BACK.
Patient problems: Bone Fracture(s)
MAUDE report 24638572 ↗InjuryMar 19, 2026Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER ALLEGES CHAIR WAS TILTED BACK AND HEARD A POP AND BACK GAVE WAY ALLEGEDLY CAUSING THE CHAIR TO FLIP BACK.
Patient problems: Bone Fracture(s)
MAUDE report 24637841 ↗InjuryJun 14, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES TIPPING WHEELCHAIR BACK TO POSITION TO GET WOUND CHANGES AND THE WHEELCHAIR FLIPPED BACKWARDS.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Bruise/Contusion
MAUDE report 11990864 ↗
Other Wheelchair, Powered devices
- SmartDrive® MX2+Max Mobility, LLC · Wheelchair, Powered858 reports
- Permobil M3Permobil, Inc. · Wheelchair, Powered1 recall59 reports
- TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx TDXSP2-MCGInvacare Corporation · Wheelchair, powered2 recalls2 reports
- TDX SP2 with LiNX Electronics TDXSP2Invacare Corporation · Wheelchair, powered2 recalls0 reports
- Invacare® TDX SP2 with Captain's Seat TDXSP2VInvacare Corporation · Wheelchair, powered2 recalls0 reports
- Q6 Edge 3Pride Mobility Products Corp · Wheelchair, Powered4 deaths86 reports
- Q6 Edge 2.0 Q6 Edge 2.0 / Q6 Edge 2.0 with iLevelPride Mobility Products Corp · Wheelchair, Powered1 death83 reports
- Permobil M5Permobil, Inc. · Wheelchair, Powered1 recall7 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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