WECK IPN915126Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 24026704696202), received between Apr 15, 2021 and Apr 15, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Entrapment of Device” (1 report).

1 other recall cover devices cleared under the same FDA submission (K132658); 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.

• InjuryApr 15, 2021Entrapment of Device; Entrapment of Device

  THEY NOTED THIS ONE HOWEVER SEEMS THAT ITS HAPPENED A FEW TIMES PERIODICALLY. WHEN THE SURGEON CLAMPS DOWN PART STAYS ON THE VESSEL OTHER STAYS ON THE APPLIER. APPLIERS IN INVENTORY ARE 533150 AND 533151. NOTHING FELL INSIDE THE PATIENT. THE CLIP STICKS AND THEN THE VESSEL GETS TORN. THE SURGEON NEEDS TO PUT MORE CLIPS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11670403 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K132658. One submission often covers many models, so check the product and lot details in each record.

• Z-1663-2023 · Apr 28, 2023 · Open, Classified
  Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or tissue ligation