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WECK IPN002001Recalls & reported problems

Teleflex Incorporated · HORIZON TI SMALL 6 Clips/Cart · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704410207), received between Jul 11, 2022 and Jul 11, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Activation Failure” (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

Device problems

  • Activation Failure1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJul 11, 2022Activation Failure; Activation Failure

    CLIPS WILL NOT STAY LOADED ON APPLIERS. 3 APPLIERS TRIED WITH FAILURE. NEW LOT' WORKED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14982254 ↗

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

Other CLIP, IMPLANTABLE devices

All CLIP, IMPLANTABLE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.