WECK IPN920969Recalls & reported problems
Teleflex Incorporated · HEMOLOK L 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 14026704725721), received between Feb 18, 2026 and Feb 18, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Migration” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Migration1
Patient problems
- Alteration in Body Temperature1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 18, 2026Migration
IT WAS REPORTED THAT, "THERE WERE 3 CLIPS, HEMOLOK CLIP AND METAL CLIP THAT WERE APPLIED ON THE RENAL ARTERY OF A LIVING DONOR. THE CLIPS SLIPPED AND OUT OF THE THREE CLIPS ONLY ONE REMAINED. THE HEMORRHAGE WAS CONTROLLED AND THE SUTURE WAS DONE WITH A THREAD". NO REPORT OF PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS "FINE".
Patient problems: Alteration in Body Temperature
MAUDE report 24377059 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.