WECK IPN920966Recalls & reported problems
Teleflex Incorporated · HEMOLOK MED 6 Clips/Cart · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 14026704725691), received between Feb 5, 2026 and Feb 5, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Failure to Seal” (3 reports).
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
- Failure to Seal3
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Hematoma1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryFeb 5, 2026Failure to Seal
IT WAS REPORTED THAT "CLAMPS FAILED. WE HAVE HAD AN INCREASED NUMBER OF FAILED VASECTOMIES WITH THE USE OF THIS LOT NUMBER IN PARTICULAR". ADDITIONAL INFORMATION RECEIVED ON JANUARY 21, 2026, INDICATED THAT "THE FAILURE WAS RELATED TO CLIP LOADING/SEATING ISSUES AND LIGATION FAILURE. THE PATIENT REQUIRED A SECOND VASECTOMY AND HAD TO VISIT THE EMERGENCY ROOM (ER) DUE TO A LARGE HEMATOMA, AFTER THE CLIP HAD TO BE CLAMPED MULTIPLE TIMES. THE PATIENT'S CURRENT CONDITION IS FINE, BUT FRUSTRATED." THREE PATIENTS WERE INVOLVED. ASSOCIATED MDRS: 3003898360-2026-00065, 3003898360-2026-00067.
Patient problems: Hematoma
MAUDE report 24274235 ↗MalfunctionFeb 5, 2026Failure to Seal
IT WAS REPORTED THAT "CLAMPS FAILED. WE HAVE HAD AN INCREASED NUMBER OF FAILED VASECTOMIES WITH THE USE OF THIS LOT NUMBER IN PARTICULAR". ADDITIONAL INFORMATION RECEIVED ON JANUARY 21, 2026, INDICATED THAT "THE FAILURE WAS RELATED TO CLIP LOADING/SEATING ISSUES AND LIGATION FAILURE. THE PATIENT REQUIRED A SECOND VASECTOMY. THE PATIENT'S CURRENT CONDITION IS FINE, BUT FRUSTRATED." THREE PATIENTS WERE INVOLVED. ASSOCIATED MDRS: 3003898360-2026-00065, ., AND 3003898360-2026-00066.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24274176 ↗MalfunctionFeb 5, 2026Failure to Seal
IT WAS REPORTED THAT "CLAMPS FAILED. WE HAVE HAD AN INCREASED NUMBER OF FAILED VASECTOMIES WITH THE USE OF THIS LOT NUMBER IN PARTICULAR". ADDITIONAL INFORMATION RECEIVED ON JANUARY 21, 2026, INDICATED THAT "THE FAILURE WAS RELATED TO CLIP LOADING/SEATING ISSUES AND LIGATION FAILURE. THE PATIENT REQUIRED A SECOND VASECTOMY AND HAD TO VISIT THE EMERGENCY ROOM (ER) DUE TO A LARGE HEMATOMA, AFTER THE CLIP HAD TO BE CLAMPED MULTIPLE TIMES. THE PATIENT'S CURRENT CONDITION IS FINE, BUT FRUSTRATED." THREE PATIENTS WERE INVOLVED. ASSOCIATED MDRS: 3003898360-2026-00067 AND 3003898360-2026-00066.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24274160 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.