WECK IPN039592Recalls & 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 24026704663846), received between Jul 24, 2024 and Jul 24, 2024 — classified as 1 malfunction.
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
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 24, 2024
ELDERLY MALE WITH HISTORY OF PROSTATE CANCER. PROCEDURE: ROBOT ASSISTED RADICAL PROSTATECTOMY WITH PELVIC NODE DISSECTION. HEM-O-LOCK LARGE CLIPS DID NOT CLIP. ANOTHER CLIP USED WITHOUT DIFFICULTY. NO KNOWN HARM TO PATIENT. CLIPS WERE NOT SAVED BUT PACKAGING WAS. MANUFACTURER RESPONSE FOR HEM-O LOCK LARGE CLIP, WECK HEM-O-LOK L (PER SITE REPORTER) UNKNOWN.
Patient problems: Insufficient Information
MAUDE report 19816477 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.