Candy Cane 4mm x 26cm Large Handle Cannula CCC426LRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00081317020899), received between Feb 14, 2019 and Mar 23, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Device Damaged Prior to Use” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 23, 2022Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT A CANNULA BENT DURING BREAST LIFT AND AXILLA LIPO. THE DEVICE WAS A CANDYCANE 4MM 26CM LG LARGE HANDLE CANNULA ON WHICH THE CANULA BENT DURING SURGERY. THE CANULA WAS BENT AT THE NECK OF HANDLE AND TIP. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13870201 ↗
• MalfunctionFeb 19, 2019Device Damaged Prior to Use; Device Damaged Prior to Use

  IT WAS REPORTED A CANNULA THAT GOT BROKE BY THE SURGEON IN THE FACILITY. NO PATIENT INVOLVEMENT REPORTED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8350455 ↗
• MalfunctionFeb 14, 2019Material Deformation; Material Deformation

  IT WAS REPORTED THAT A CANNULA WAS DAMAGED BY A SURGEON IN THE FACILITY. THE DEVICE WAS A CANDY CANE 4MM X 26CM LARGE HANDLE CANNULA ON WHICH THE TIP WAS BROKEN. THERE WAS NO PATIENT INVOLVEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8341717 ↗