DRIVEMEDICAL K318DFA-ELRRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383133881), received between Aug 15, 2024 and Aug 15, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Mechanical Problem” (1 report).

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryAug 15, 2024Mechanical Problem; Mechanical Problem

  DRIVE DEVILBISS WAS NOTIFIED OF AN INCIDENT INVOLVING A WHEELCHAIR BY THE END USER WHO STATED THAT SHE WAS ATTEMPTING TO TRANSFER FROM THE BED TO THE WHEELCHAIR USING A TRANSFER BOARD WHEN THE WHEELCHAIR MOVED CAUSING HER TO FALL TO THE FLOOR. THE END USER CLAIMS THAT THE BRAKES WERE ENGAGED AT THE TIME OF THE EVENT AND CLAIMS THERE IS AN" ISSUE WITH THE BRAKES." THE END USER SUSTAINED BRUISING TO HER RIGHT HIP AND LEGS AND BOTH FEET AND ANKLES WERE SWOLLEN. THE END USER WAS HOSPITALIZED AND IS NOW IN A REHABILITATION FACILITY. 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: Swelling/ Edema

  MAUDE report 19991286 ↗