Mercedes 2mm x 15cm Small Handle Cannula MER215SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00081317021407), received between Mar 31, 2023 and Apr 27, 2023 — classified as 2 malfunctions.

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 27, 2023Break; Break

  IT WAS REPORTED THAT A MERCEDES 2MM X 15CM SMALL HANDLE CANNULA WAS BEING UTILIZED IN AN UNSPECIFIED PROCEDURE. DURING THE PROCEDURE, THE CANNULA TIP BROKE OFF INSIDE OF A PATIENT. THE TIP WAS REMOVED, AND NO SURGICAL DELAYS OR PATIENT CONSEQUENCES WERE REPORTED. SEVERAL FOLLOW-UPS HAVE BEEN CONDUCTED, AND NO ADDITIONAL INFORMATION HAS BEEN RECEIVED. IF MORE INFORMATION BECOMES AVAILABLE, MENTOR WILL SUBMIT A SUPPLEMENTAL REPORT ACCORDINGLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16823983 ↗
• MalfunctionMar 31, 2023Break; Break

  IT WAS REPORTED THAT A MERCEDES 2MM X 15CM SMALL HANDLE CANNULA BEING USED IN A LIPOSUCTION SURGERY BROKE AT THE TIP DURING THE OPERATION. NO ADVERSE EVENT WAS EXPERIENCED BY THE PATIENT AND NO PATIENT CONSEQUENCES WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16658400 ↗