Becker Tear Drop 3mm x 26cm Large Handle Cannula BECTD326LRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00081317020752), received between Feb 8, 2022 and Aug 24, 2022 — 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.

• MalfunctionAug 24, 2022Break; Break

  IT WAS REPORTED THAT A BECKER TEAR DROP 3MM X 26CM LARGE HANDLE CANNULA HAD A BROKEN PRONG TIP POST-OPERATIVELY. NO PATIENT CONSEQUENCES, ADVERSE EVENT OR DELAYS DURING THE PROCEDURE WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15285504 ↗
• MalfunctionFeb 8, 2022Break; Material Twisted/Bent; Break; Material Twisted/Bent

  IT WAS REPORTED THAT A BECKER TEAR DROP 3MM X 26CM LARGE HANDLE CANNULA WAS BEING UTILIZED IN AN UNSPECIFIED PROCEDURE. DURING THE PROCEDURE ONE OF THE THREE PRONGS BECAME BENT AND BROKE OFF OF THE DEVICE. NO PATIENT CONSEQUENCES OR DELAYS DURING THE PROCEDURE WERE REPORTED. THE DEVICE WAS DISCARDED AND A REPLACEMENT WAS ORDERED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13481138 ↗