Drive AK518ADA-AELRRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00822383136639), received between Aug 25, 2021 and Aug 25, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Sharp Edges” (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 16, 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 25, 2021Sharp Edges; Sharp Edges

  DRIVE DEVILBISS HEALTHCARE IS THE INITIAL IMPORTER OF THE DEVICE WHICH IS A WHEELCHAIR. THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. WE ARE FILING THIS REPORT IN AN OVERABUNDANCE OF CAUTION. WE WILL FILE A FOLLOW-UP WHEN ADDITIONAL INFORMATION IS AVAILABLE. THE LEG REST WAS DETACHED FROM THE DEVICE AT THE TIME OF THE INCIDENT THE FRONT LG POST CAME DOWN AND WAS OPEN ENDED. IT CUT THE USER'S LEG. THEY SOUGHT MEDICAL ATTENTION AT THE FACILITY WHERE THE NURSE CAME TO BANDAGE AND CLEAN UP LIQUID DRAINING FROM THE CUT. THE USER'S LEG IS SWOLLEN NO STITCHES WERE REQUIRED. A BIG BANDAGE PATCH WAS APPLIED TO STOP THE BLEEDING.

  Patient problems: Laceration(s)

  MAUDE report 12365761 ↗