WECK IPN920983Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704725363), received between Feb 4, 2026 and Feb 4, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Sharp Edges” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• MalfunctionFeb 4, 2026Sharp Edges

  IT WAS REPORTED THAT "INSTEAD OF CLIPPING THE ARTERIES, THE CLIP CUT THEM, BEING THEN EXTREMELY DANGEROUS AND DAMAGING DURING CORONARY AND MAMMARY ARTERY SURGERY. THE USE OF THESE CLIPS HAS BEEN IMMEDIATELY DISCONTINUED AT THE SURGEON'S REQUEST. WE WILL BE USING AN OLDER REFERENCE OF APPLIER AND CLIPS." MULTIPLE ATTEMPTS FOR ADDITIONAL INFORMATION HAVE BEEN REQUESTED FROM THE COMPLAINANT HAVE BEEN UNSUCCESSFUL AT THE TIME OF THIS REPORT.

  Patient problems: Insufficient Information

  MAUDE report 24264248 ↗

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