WECK IPN915188Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 24026704709902), received between Feb 18, 2021 and Jul 13, 2023 — classified as 3 malfunctions.

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

• MalfunctionJul 13, 2023Failure to Align; Failure to Align

  IT WAS REPORTED THAT "THE JAWS OF THE APPLIER WERE FOUND MISALIGNED DURING A SURGERY. THEREFORE, ANOTHER APPLIER WAS USED TO COMPLETE THE PROCEDURE. NO CLIP FELL/REMAINED IN THE PATIENT". NO PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "FINE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17318163 ↗
• MalfunctionMar 29, 2023Fracture; Fracture

  REPORTED ISSUE: BLOCKAGE AND BREAKAGE OF ONE OF THE JAWS DURING USE IN A PATIENT'S ABDOMEN. NO REPORTED INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16639590 ↗
• MalfunctionFeb 18, 2021Difficult to Remove; Difficult to Remove

  NO PATIENT HARMED, OR REPORTED IN THIS INCIDENT. CSSD MANAGER REPORTED THAT SURGEON COMMUNICATED THE APPLIER IS NOT WORKING PROPERLY AND BELIEVES THERE IS AN ISSUE WITH THE HANDLE. ADDITIONAL INFORMATION: THE CLIP WOULD LOAD NORMALLY. THE ISSUE PRESENTED ONCE THE CLIP WAS PLACED, THE JAWS WOULD NOT RELEASE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11342683 ↗