WECK IPN005033Recalls & reported problems
Teleflex Incorporated · HORIZON ENDOSCOPIC CLIP APPLIER MEDIUM-LARGE · Class 1
- 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 24026704428872), received between Nov 28, 2023 and Nov 28, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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
- Material Separation1
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.
MalfunctionNov 28, 2023Material Separation; Material Separation
THE REPORT STATES "THE ENDO APPLIER IS MISSING THE SCREW, AND THEY CANNOT SAY WHERE IT HAS GONE. COULD BE IN THE PATIENT, OR ON THE FLOOR. I ASKED IF IT COULD HAVE OCCURRED DURING CLEANING, PRIOR TO SURGERY, UNFORTUNATELY THEY HAVE NO CERTAINTY WHEN THIS HAPPENED AT THE MOMENT". AT THE TIME OF THIS REPORT, THE CUSTOMER HAS NOT RETURNED OUR REQUESTS FOR ADDITIONAL INFORMATION. IF FURTHER INFORMATION IS RECEIVED, THE COMPLAINT FILE WILL BE UPDATED.
Patient problems: Insufficient Information
MAUDE report 18222254 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.