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Scout SFSCOUT3Recalls & reported problems

Drive Devilbiss Healthcare · Scout 3-Wheel Scooter, Red/Blue · Class 2

Adverse event reports
4
Deaths reported
0
Injuries reported
4
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00822383519081), received between Feb 12, 2021 and Mar 11, 2022 — classified as 4 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

Most reported problems

Device problems

  • Insufficient Device Problem Information2
  • Adverse Event Without Identified Device or Use Problem1
  • Device Unsafe to Use in Environment1
  • Unintended Movement1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
  • Bone Fracture(s)1
  • Easy Bruising1
  • Fall1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 11, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

    WUS TECH (VIETNAM) IS THE MANUFACTURER AND DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A POWER WHEELCHAIR. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. WE WILL SUBMIT ADDITIONAL DATA WHEN IT BECOMES AVAILABLE. THE CUSTOMER STATED SHE DOESN'T THINK SHE IS SUITED FOR ONE WHEEL SCOOTERS IN THE FRONT AND IS UNHAPPY WITH THEM. WHEN SHE IS DRIVING IT THE WHEELS ARE HARD AND SHE CAN FEEL THE BUMPS AND HAS BRUISES ON HER BODY WITH EVERY STEP. THE END-USER WAS ATTEMPTING TO MAKE A LEFT TURN WHILE USING THE DEVICE. SHE REPORTED THAT THE WHEELS GOT STUCK AND SHE TRIED TO STOP THE MOMENTUM OF THE DEVICE WIT HER LEFT LEG. THERE WAS SOME SWELLING OF THE LEG AND COMPLAINED THAT HER BONES HURT. SHE WENT TO THE HOSPITAL FOR X-RAYS. A SECOND INCIDENT OCCURRED WHILE SHE WAS GOING TO THERAPY WITH THE SCOOTER. SHE CAME OFF THE BUS AND TURNED RIGHT TO CROSS THE STREET. WHEN SHE TURNED TO HER LEFT THE DEVICE FLIPPED OVER AND LANDED ON HER. SHE WENT TO THE DOCTOR THERE WAS SOME BRUISING AND SWELLING ON THE CUSTOMERS LEGS AND HIP. THE END USER WILL DO PHYSICAL THERAPY ON HER LEG.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 13728610 ↗
  • InjuryMar 1, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

    WUS TECH (B)(4) CO., LTD. IS THE MANUFACTURER OF THE DEVICE WHICH IS A THREE-WHEELED POWER MOBILITY DEVICE, AND (B)(4) HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE. THE PRODUCT HAS NOT BEEN RETURNED FOR EVALUATION. THE END-USER CONFIRMS THAT THERE IS NOTHING WRONG WITH THE DEVICE, HOWEVER SHE WANTS A FOUR WHEELED SCOOTER AS REPLACEMENT. THE THREE-WHEELED SCOOTER TIPPED OVER WHILE USER WAS CHECKING HER MAIL. SHE WAS RIDING DOWN AN INCLINE AND THE DEVICE FELL ON TOP OF HER. SHE BROKE A RIB. SHE CONFIRMED THAT NOTHING IS WRONG WITH THE SCOOTER SHE WANTS A REPLACEMENT SINCE SHE BELIEVES SHE SHOULD HAVE BEEN GIVEN A FOUR WHEELED ONE IN THE FIRST PLACE.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 13627778 ↗
  • InjuryOct 18, 2021Unintended Movement; Unintended Movement

    DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A POWER WHEELCHAIR. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. WE WILL SUBMIT ADDITIONAL DATA WHEN IT BECOMES AVAILABLE. THE CUSTOMER STATED SHE DOESN'T THINK SHE IS SUITED FOR ONE WHEEL SCOOTERS IN THE FRONT AND IS UNHAPPY WITH THEM. WHEN SHE IS DRIVING IT THE WHEELS ARE HARD AND SHE CAN FEEL THE BUMPS AND HAS BRUISES ON HER BODY WITH EVERY STEP. THE END-USER WAS ATTEMPTING TO MAKE A LEFT TURN WHILE USING THE DEVICE. SHE REPORTED THAT THE WHEELS GOT STUCK AND SHE TRIED TO STOP THE MOMENTUM OF THE DEVICE WIT HER LEFT LEG. THERE WAS SOME SWELLING OF THE LEG AND COMPLAINED THAT HER BONES HURT. SHE WENT TO THE HOSPITAL FOR X-RAYS A SECOND INCIDENT OCCURRED WHILE SHE WAS GOING TO THERAPY WITH THE SCOOTER. SHE CAME OFF THE BUS AND TURNED RIGHT TO CROSS THE STREET . WHEN SHE TURNED TO HER LEFT THE DEVICE FLIPPED OVER AND LANDED ON HER. SHE WENT TO THE DOCTOR THERE WAS SOME BRUISING AND SWELLING ON THE CUSTOMERS LEGS AND HIP. THE END USER WILL DO PHYSICAL THERAPY ON HER LEG.

    Patient problems: Easy Bruising; Fall

    MAUDE report 12646691 ↗
  • InjuryFeb 12, 2021Device Unsafe to Use in Environment; Adverse Event Without Identified Device or Use Problem; Device Unsafe to Use in Environment; Adverse Event Without Identified Device or Use Problem

    (B)(4) HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A THREE-WHEELED POWER MOBILITY DEVICE. THE PRODUCT HAS NOT BEEN RETURNED FOR EVALUATION. THE END-USER CONFIRMS THAT THERE IS NOTHING WRONG WITH THE DEVICE, HOWEVER SHE WANTS A FOUR WHEELED SCOOTER AS REPLACEMENT. THE THREE-WHEELED SCOOTER TIPPED OVER WHILE USER WAS CHECKING HER MAIL. SHE WAS RIDING DOWN AN INCLINE AND THE DEVICE FELL ON TOP OF HER. SHE BROKE A RIB. SHE CONFIRMED THAT NOTHING IS WRONG WITH THE SCOOTER SHE WANTS A REPLACEMENT SINCE SHE BELIEVES SHE SHOULD HAVE BEEN GIVEN A FOUR WHEELED ONE IN THE FIRST PLACE.

    Patient problems: Bone Fracture(s)

    MAUDE report 11324217 ↗

Other VEHICLE, MOTORIZED 3-WHEELED devices

All VEHICLE, MOTORIZED 3-WHEELED devices →

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