WECK IPN920973Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704725288), received between May 6, 2026 and May 6, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Seal” (1 report).

1 other recall cover devices cleared under the same FDA submission (K982313); they may or may not involve this specific model.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 6, 2026Sharp Edges; Failure to Seal

  IT WAS REPORTED THAT "AN INCIDENT OCCURRED ON 31 MARCH 2026 WITH A HORIZON DEVICE. HORIZON APPLIER & CLIP CUT THE PATIENT'S VESSELS INSTEAD OF LIGATING THEM". THE PATIENT'S CURRENT CONDITION IS REPORTED AS UNKNOWN. ADDITIONAL INFORMATION WAS REQUESTED FROM THE CUSTOMER; HOWEVER, FURTHER DETAILS FROM THE CUSTOMER HAS NOT BEEN PROVIDED AT THIS TIME.

  Patient problems: Perforation of Vessels

  MAUDE report 25093272 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K982313. One submission often covers many models, so check the product and lot details in each record.

• Z-2327-2016 · Aug 8, 2013 · Terminated
  Horizon 24 Large Titanium Clips with Adhesive Backing, Ref 004204, Rx Only, Sterile. The metal ligating clips are intended for use in procedures involving vessels or anatomic stru