Quickie Q300MRecalls & reported problems
Sunrise Medical (US) LLC · Go where others can't with the Q300 M Mini: the narrowest TRUE mid-wheel drive QUICKIE power wheelchair with an ultra-small 17" turning radius. Enjoy a safe and comfortable ride with patented all-wheel suspension that independently cushions every wheel. Climb obstacles of up to 3" with 12" drive wheels. Power through tricky terrain with strong, energy efficient 4-pole motors. Plus, the Q300 M Mini has a multi-adjustable seating system and a whole host of styling options. · Class 2
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00016958060485), received between Dec 14, 2021 and Apr 23, 2026 — classified as 5 injuries.
The most frequently reported specific device problem is “Device Handling Problem” (2 reports).
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Device Handling Problem2
- Device Tipped Over2
- Improper or Incorrect Procedure or Method2
- Use of Device Problem2
- Appropriate Device Problem Term/Code Not Available1
- Insufficient Device Problem Information1
Patient problems
- Bone Fracture(s)2
- Fall2
- Head Injury1
- Insufficient Information1
- Laceration(s)1
- Limb Fracture1
- Limb Pain1
- Muscle/Tendon Damage1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryApr 23, 2026Adverse Event Without Identified Device or Use Problem
PER (B)(6), USER IS (B)(6), CLAIMING INJURY DUE TO UNEXPECTED ACCELERATION BY THE WHEELCHAIR. DOCUMENTS HAVE BEEN FORWARDED. USER IS (B)(6), BORN 1954. (B)(6).
Patient problems: Laceration(s)
MAUDE report 24974215 ↗InjuryApr 15, 2026Use of Device Problem; Improper or Incorrect Procedure or Method; Device Tipped Over; Device Handling Problem
A DISTRIBUTOR REPORTED THAT AN END USER, WHO HAS A HISTORY OF MULTIPLE PRIOR ACCIDENTS WITHIN A SIX-MONTH PERIOD (INCLUDING INJURIES LEADING TO WHEELCHAIR USE), WAS INVOLVED IN A RECENT INCIDENT WHILE TRAVELING IN A MOBILITY TAXI. THE WHEELCHAIR WAS NOT PROPERLY SECURED, AND THE VEHICLE WAS T-BONED, RESULTING IN THE END USER BEING EJECTED FROM THE CHAIR, WITH THE CHAIR SUBSEQUENTLY LANDING ON HIM. THE END USER WAS TAKEN TO THE HOSPITAL AND SUSTAINED RIB FRACTURES. THE EXACT DATE OF THE INCIDENT IS CURRENTLY UNKNOWN. THE DISTRIBUTOR INDICATED INTENT TO REQUEST REPLACEMENT PARTS; HOWEVER, EVALUATION OF THE WHEELCHAIR'S STRUCTURAL INTEGRITY IS PENDING PRIOR TO FURTHER ACTION.
Patient problems: Bone Fracture(s)
MAUDE report 24884686 ↗InjuryAug 14, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
SUMMONS WAS RECEIVED BY SUNRISE MEDICAL ON (B)(6) 2025 OF AN INJURY TO A 69 YEAR OLD END USER THAT TOOK PLACE IN EARLY (B)(6) 2024 (NO EXACT DATE OF INJURY WAS GIVEN, (B)(6) IS BEING USED AS EARLIEST POSSIBLE DATE). ACCORDING TO THE DETAILS PROVIDED IN THE SUMMONS, THE END USER ATTEMPTED TO SIT FORWARD SLIGHTLY TO READ A DOCUMENT, AND THE USER'S FOOT SLIPPED OFF THE FOOTPLATE, SHE BECAME UNSTABLE AND FELL FORWARD OUT OF THE WHEELCHAIR. IT WAS REPORTED THAT THE END USER SUSTAINED AN INJURY TO THE FEMUR. THIS INCIDENT IS STATED TO HAVE OCCURRED WITHIN HOURS AFTER THE DEALER'S TECHNICIAN MADE ADJUSTMENTS TO THE CHAIR.
Patient problems: Bone Fracture(s); Fall; Insufficient Information; Limb Pain
MAUDE report 22801649 ↗InjuryJun 7, 2025Use of Device Problem; Improper or Incorrect Procedure or Method; Device Tipped Over; Device Handling Problem; Use of Device Problem; Improper or Incorrect Procedure or Method; Device Tipped Over; Device Handling Problem
PER PHONE CALL FROM THE DEALER, (B)(6), THE USER CLAIMS THAT ON SATURDAY, 5/3, WHILE CROSSING A CROSS WALK, THE USER'S FOOTPLATE WAS EXTREMELY LOW TO THE FLOOR AND HIT A ROAD REFLECTOR. THE CHAIR TIPPED ON ITS RIGHT SIDE CAUSING AN INJURY. PER THE USER, THE INJURIES WERE TO THE HEAD (RESULTING IN 5 STITCHES), A TORN RIGHT-SIDE ACL, RIGHT SIDE TORN LIGAMENT IN THE RIGHT KNEE AND AN INJURY TO THE RIGHT TIBIA. PER THE USER, THERE WERE NO ENVIRONMENTAL FACTORS THAT CAUSED THE CHAIR TO FALL OVER. THE USER WAS TAKEN TO THE ER ON SATURDAY. PER THE USER, THEY WERE ALSO SEEN BY THEIR ORTHOPEDIC DR ON THE DAY OF THE REPORT TO SUNRISE MEDICAL.
Patient problems: Head Injury; Muscle/Tendon Damage; Rupture
MAUDE report 22163060 ↗InjuryDec 14, 2021Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available; Adverse Event Without Identified Device or Use Problem; Appropriate Device Problem Term/Code Not Available
END USER REPORTED THAT HE WAS ATTEMPTING TO DRIVE HIS CHAIR ONTO A LIFT. WHEN HE MOVED HIS CHAIR UP THE SMALL RAMP OF THE LIFT, THE WHEELS SPUN OUT, THE CHAIR WENT OFF THE LEFT SIDE OF THE LIFT, AND HE SUBSEQUENTLY FELL OUT OF THE CHAIR. AT THAT TIME HE DID NOT SEEK MEDICAL ATTENTION, BUT ON (B)(6) 2021 WENT TO SEE A DOCTOR FOR AN UNRELATED ISSUE, HAD HIS ARM X-RAYED, AND DISCOVERED A BROKEN LEFT HUMERUS.
Patient problems: Fall; Limb Fracture
MAUDE report 13006554 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.