WECK IPN928364Recalls & reported problems
Teleflex Incorporated · HEMOLOK ML 6 Clips/Cart · Class 2 · Implant
All models of WECK (97)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 14026704917034), received between Mar 13, 2026 and Mar 13, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Device Slipped” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Device Slipped1
Patient problems
- Hemorrhage/Blood Loss/Bleeding1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 13, 2026Device Slipped
THE HEALTHCARE FACILITY INITIALLY REPORTED ON (B)(6) 2026, "POST-OPERATIVE DAY 0, THE PATIENT WAS RETURNED TO THE OPERATING THEATRE (OT) FOR EMERGENCY INTERVENTION DUE TO BLEEDING. FINDINGS: UPON RE-ENTRY, IT WAS NOTED THAT CYSTIC DUCT STUMP CLIPS WERE IN SITU; HOWEVER, CYSTIC ARTERY CLIPS WERE OPENED WITH BLEEDING FROM THE CYSTIC ARTERY STUMP." LATER ON (B)(6) 2026, THE HEALTHCARE FACILITY REPORTED, "UNFORTUNATELY, THE PATIENT HAS PASSED AWAY. PATIENT BLED MASSIVELY WITH HEMOPERITONEUM REQUIRING SURGERY. PATIENT HAD AT LEAST 3 CYCLES OF MASSIVE TRANSFUSION PROTOCOL (12UNITS OF PTC)." ON (B)(6) 2026, THE HEALTHCARE FACILITY REPORTED "THE TWO HEMOLOK CLIPS IN QUESTION WERE DISLOGED RATHER THAN "OPEN" AS PREVIOUSLY STATED."
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 24591729 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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