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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 1 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 2 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

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 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.