Becker 5mm x 26cm Large Handle Cannula BEC526LRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00081317020745), received between Mar 12, 2019 and Aug 25, 2022 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 25, 2022Break; Break

  IT WAS REPORTED THAT A 26CM LG BECKER 5MM X 26CM LARGE HANDLE CANNULA BROKE WHILE IN USE INSIDE OF THE PATIENT INTRA-OPERATIVELY. THE TIP OF THE LIPOSUCTION HANDPIECE BROKE. NO PATIENT CONSEQUENCE OR PROCEDURAL DELAYS WERE REPORTED. FURTHERMORE, NO SERIOUS INJURY WAS REPORTED. THIS EVENT WAS REPORTED TO THE FDA UNDER MW: (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15299044 ↗
• InjuryMar 12, 2019Material Separation; Material Separation

  IT WAS REPORTED THAT A PATIENT UNDERWENT A SURGERY OF UNKNOWN TYPE WITH A BECKER 5MM X 26CM LARGE HANDLE CANNULA 5MM X 26CM AND TIP BROKE OFF IN THE PATIENT DURING LIPOSUCTION SURGERY. THE HEALTHCARE PROFESSIONAL HAD TO FIND IT WITH X-RAY AND THEREFORE, HAD TO MAKE ANOTHER INCISION. THE PATIENT DID NOT EXPERIENCE ANY INJURY.

  Patient problems: No Code Available

  MAUDE report 8415039 ↗