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DRIVEMEDICAL GV974HD-BRRecalls & reported problems

Drive Devilbiss Healthcare · RollatorsBariatric Product Description: F22 Rollator, HD, Black · Class 1

All models of DRIVEMEDICAL (111)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
7
Deaths reported
1
Injuries reported
6
Recalls naming it
0

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00822383582245), received between Feb 19, 2020 and Apr 14, 2026 — classified as 1 death, 6 injuries.

The most frequently reported specific device problem is “Break” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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: 0 reportsJul 2025: 0 reportsAug 2025: 0 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

  • Break2
  • Mechanical Problem2
  • Fracture1
  • Material Fragmentation1
  • Material Integrity Problem1

Patient problems

  • Fall5
  • Concussion2
  • Vertebral Fracture2
  • Bone Fracture(s)1
  • Bruise/Contusion1
  • Damage to Ligament(s)1

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 14, 2026Mechanical Problem

    PER DRIVE DEVILBISS HEALTHCARE MDR 2438477-2026-00020: DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY THE END USER WHO STATED THAT THE BACKREST BRACKET BROKE DURING USE CAUSING HER TO FALL. SHE WAS EVALUATED AT THE EMERGENCY ROOM AND WAS DIAGNOSED WITH A MILD CONCUSSION. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

    Patient problems: Concussion

    MAUDE report 24870777 ↗
  • InjuryApr 10, 2026Mechanical Problem

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY THE END USER WHO STATED THAT THE BACKREST BRACKET BROKE DURING USE CAUSING HER TO FALL. SHE WAS EVALUATED AT THE EMERGENCY ROOM AND WAS DIAGNOSED WITH A MILD CONCUSSION. AS PART OF ITS COMPLAINT REVIEW AND EVALUATION PROCESS, DRIVE DEVILBISS HEALTHCARE WILL ALSO NOTIFY THE MANUFACTURER OF THE PRODUCT ABOUT THIS COMPLAINT.

    Patient problems: Concussion

    MAUDE report 24845342 ↗
  • InjuryApr 21, 2023Break; Break

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY AN END USER, WHO STATED THAT HE WAS SITTING ON THE ROLLATOR WHEN "THE BACK SUPPORT SUDDENLY BROKE (SUPPORT SCREW DISLODGED)." THE END USER REPORTED THAT HE WAS "THROWN TO THE FLOOR," SUSTAINING A SPRAINED ELBOW AND SPINE LIGAMENT, AND SOUGHT MEDICAL TREATMENT AS A RESULT OF THE INCIDENT. MULTIPLE ATTEMPTS TO GATHER FURTHER INFORMATION HAVE BEEN MADE, AND TO RETRIEVE THE PRODUCT FOR EVALUATION, BUT DRIVE HAS NOT RECEIVED A RESPONSE. DRIVE WILL CONTINUE TO MONITOR COMPLAINTS FOR ANY RELATED TRENDS.

    Patient problems: Damage to Ligament(s); Fall

    MAUDE report 16788012 ↗
  • InjuryApr 19, 2023Break; Break

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY AN END USER, WHO STATED THAT THE "BACKREST BROKE, AND HE FELL AND BROKE HIS BACK, SPRAINED HIS WRISTS, LOWER BACK, AND RIGHT KNEE." HE DID NOT PROVIDE ANY FURTHER INFORMATION ABOUT HOW THE ROLLATOR WAS BEING USED AT THE TIME OF THE INCIDENT. THE END USER WAS REPORTEDLY TAKEN TO THE HOSPITAL BY AMBULANCE TO TREAT HIS INJURIES. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

    Patient problems: Fall; Vertebral Fracture

    MAUDE report 16771424 ↗
  • DeathDec 23, 2022Fracture; Fracture

    DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY AN END USER'S WIFE, WHO STATED THAT "HE WAS SITTING IN THE PRODUCT WITH THE WHEEL LOCKS ENGAGED WHEN THE CROSS-FRAME SNAPPED CAUSING HIM TO ABRUPTLY COLLAPSE DOWNWARD WITH THE SIDES CLOSING IN ON HIM". THE END USER WAS TAKEN TO THE HOSPITAL WHERE HE WAS REPORTEDLY DIAGNOSED WITH BRUISED RIBS AND MULTIPLE VERTEBRAE FRACTURES. END USER DIED SEVERAL DAYS LATER. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

    Patient problems: Bruise/Contusion; Fall; Vertebral Fracture

    MAUDE report 16043199 ↗
  • InjurySep 20, 2022Material Integrity Problem; Material Integrity Problem

    NORA REVISION: DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED BY A DISTRIBUTOR OF AN INCIDENT INVOLVING A ROLLATOR, IN WHICH AN ATTORNEY STATED THAT THE END USER REPORTEDLY FELL DUE TO A "DEFECTIVE PLASTIC PIECE THAT IS TO ATTACH TO THE BACKREST." THE END USER REPORTEDLY HIT HIS NECK AND BACK, FOR WHICH HE SOUGHT MEDICAL ATTENTION. DRIVE IS CURRENTLY INVESTIGATING THE INCIDENT, INCLUDING ATTEMPTING TO RETRIEVE THE PRODUCT AND INSPECT IT, AND WILL FILE AN UPDATE IF ADDITIONAL INFORMATION BECOMES AVAILABLE.

    Patient problems: Fall

    MAUDE report 15457065 ↗
  • InjuryFeb 19, 2020Material Fragmentation; Material Fragmentation

    DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. THE END USER SAT ON THE DEVICE. THE REAR LEFT WHEEL OF THE PRODUCT REPORTEDLY DETACHED AND HE FELL BACKWARDS HE WAS UNCONSCIOUS FOR ABOUT 20 MINUTES. HE ENDED UP BEING DIAGNOSED WITH A FRACTURED T7 VERTEBRA. A PROCEDURE CALLED A KYPHOPLASTY WAS RECOMMENDED BUT HE ELECTED NOT TO UNDERGO SURGERY AT THIS TIME AND IS INSTEAD JUST TREATING WITH PT.

    Patient problems: Bone Fracture(s); Fall

    MAUDE report 9728741 ↗

Other WALKER, MECHANICAL devices

All WALKER, MECHANICAL devices →

Sources and updates

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