WECK IPN915128Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 24026704696226), received between Mar 30, 2022 and Mar 30, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (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.

• MalfunctionMar 30, 2022Material Split, Cut or Torn; Material Split, Cut or Torn

  OPERATING ROOM HAS FOUND THE OUTER PLASTIC PACKAGE OF ITEM 533862 WITH A HOLE IN IT. PRODUCT DEFECT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13952501 ↗

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