WECK IPN028128Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 34026704625209), received between Feb 10, 2021 and Jul 25, 2023 — classified as 2 malfunctions.

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. How this data works · Data updated Oct 13, 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.

• MalfunctionJul 25, 2023Difficult to Open or Close; Difficult to Open or Close

  IT WAS REPORTED THAT "THE CLIP DOES NOT CLOSE DURING USAGE ON THE PATIENT. THEN USE ANOTHER CLIP (THE SAME BATCH). MORE INFORMATION IS CURRENTLY UNKNOWN, PENDING SALES FOLLOW-UP." NO PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "FINE". AT THE TIME OF THIS REPORT, THE CUSTOMER HAS NOT RETURNED OUR REQUESTS FOR ADDITIONAL INFORMATION. IF FURTHER INFORMATION IS RECEIVED, THE COMPLAINT FILE WILL BE UPDATED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17392765 ↗
• MalfunctionFeb 10, 2021Break; Break

  IT WAS REPORTED THAT A CLIP GOT BROKEN AT THE HOOK AT LIGATION DURING A SURGERY. THEREFORE, A NEW CARTRIDGE WAS OPENED INSTEAD. NO PART OF THE BROKEN CLIP FELL INSIDE THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11308514 ↗