DRIVEMEDICAL GV974RD-TRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00822383582238), received between Oct 8, 2018 and Mar 25, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Fracture” (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.

Most reported problems

Recent adverse event reports

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

• InjuryMar 25, 2026Fracture

  PER DISTRIBUTOR MDR #243477-2026-00015: DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY THE END USER WHO REPORTED THE WELD AT THE CROSSBAR BROKE CAUSING THE END USER TO FALL. THE END USER CAUGHT HIMSELF AND NOTICED A HERNIA THAT EVENING IN HIS GROIN AREA. THE END USER REQUIRED EMERGENCY SURGERY TO REPAIR THE HERNIA. 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: Hernia

  MAUDE report 24687747 ↗
• InjuryMar 19, 2026Fracture

  DRIVE DEVILBISS HEALTHCARE WAS NOTIFIED OF AN INCIDENT INVOLVING A ROLLATOR BY THE END USER WHO REPORTED THE WELD AT THE CROSSBAR BROKE CAUSING THE END USER TO FALL. THE END USER CAUGHT HIMSELF AND NOTICED A HERNIA THAT EVENING IN HIS GROIN AREA. THE END USER REQUIRED EMERGENCY SURGERY TO REPAIR THE HERNIA. 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: Hernia

  MAUDE report 24640574 ↗
• InjuryAug 20, 2019Break; Material Fragmentation; Break; Material Fragmentation

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHIHC IS A ROLLATOR. OUR PMS TEAM WAS ADVISED OF THIS EVENT BY AN ATTORNEY'S LETTER. WE DO NOT HAVE POSSESSION OF THE DEVICE NOR DO WE EXPECT TO IN THE NEAR FUTURE. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. THE ENUDER REPORTEDLY SUFFERED AN INJURY ON (B)(6) 2019 WHILE USING THE DEVICE. THE SUPPORTING LEG FOR A FRONT WHEEL SHEARED OFF THE PRODUCT CAUSING HER TO FALL FORWARD, FRACTURING HER WRIST.

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 8912129 ↗
• InjuryOct 8, 2018Material Fragmentation; Material Fragmentation

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A ROLLATOR. PMS IS COORDINATING THE RETURN OF THE DEVICE AND WHEEL FOR EVALUATION. END-USER WAS WALKING WITH THE DEVICE WHEN THE RIGHT WHEEL FELL OFF. HE FELL AND WAS INJURED. HE REPORTEDLY INJURED HIS SHOULDER AND NECK.

  Patient problems: Bone Fracture(s); Fall

  MAUDE report 7945234 ↗