anchor Tissue Retrieval System TRS-TV-25Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20653405986178), received between Oct 1, 2021 and Oct 1, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 1, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE TRS-TV-25 WAS USED DURING A ROBOTIC HYSTERECTOMY ON APPROXIMATELY (B)(6) 2021 WHEN IT WAS REPORTED ¿THE KICKSTAND BROKE OFF DURING PROCEDURE¿. THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR HOSPITALIZATION FOR THE PATIENT. FURTHER ASSESSMENT QUESTIONING FOUND THAT THE COMPONENT, THE METAL ARM, THAT RELEASES THE BAG HAD FALLEN INTO THE PATIENT AND WAS RETRIEVED WITH ROBOTIC GRASPERS AND PLACED IN THE BAG. THE PROCEDURE IS REPORTED AS HAVING BEEN COMPLETED AS PLANNED WITH A 5-MINUTE DELAY. THE SALES REPRESENTATIVE ALSO REPORTED THAT THE SURGEON HAD GRABBED THE ARM OF THE DEVICE TO HELP OPEN THE BAG AND THAT THIS IS THE POSSIBLE REASON FOR THE FAILURE. THE PATIENT HAS BEEN REPORTED AS DOING ¿WELL¿. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12561097 ↗