WECK IPN915141Recalls & reported problems
Teleflex Incorporated · Class 1
All models of WECK (97)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 24026704696639), received between Dec 8, 2021 and May 20, 2022 — classified as 5 injuries.
The most frequently reported specific device problem is “Positioning Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Positioning Problem3
- Mechanical Problem2
Patient problems
- Unspecified Tissue Injury3
- Insufficient Information1
- Perforation of Vessels1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2022Positioning Problem; Positioning Problem
WHEN CLOSING VESSEL WITH MICROCLIP VESSEL IS CUT.
Patient problems: Unspecified Tissue Injury
MAUDE report 14455587 ↗InjuryMay 20, 2022Positioning Problem; Positioning Problem
WHEN CLOSING VESSEL WITH MICROCLIP VESSEL IS CUT.
Patient problems: Unspecified Tissue Injury
MAUDE report 14455318 ↗InjuryMay 20, 2022Positioning Problem; Positioning Problem
WHEN CLOSING VESSEL WITH MICROCLIP VESSEL IS CUT.
Patient problems: Unspecified Tissue Injury
MAUDE report 14455162 ↗InjuryDec 8, 2021Mechanical Problem; Mechanical Problem
A SURGEON HAD ISSUES WITH OUR 537081 APPLIERS. THEY DAMMAGE THE VESSELS.
Patient problems: Perforation of Vessels
MAUDE report 12961547 ↗InjuryDec 8, 2021Mechanical Problem; Mechanical Problem
A SURGEON HAD ISSUES WITH OUR 537081 APPLIERS. THEY DAMMAGE THE VESSELS.
Patient problems: Insufficient Information
MAUDE report 12961546 ↗
Other Applier, surgical, clip devices
- LIGACLIP MCS20Ethicon Endo-Surgery, LLC · Applier, surgical, clip1 death337 reports
- Endo Clip III 176630BCovidien LP · Applier, surgical, clip312 reports
- LIGACLIP MCM20Ethicon Endo-Surgery, LLC · Applier, surgical, clip308 reports
- LIGACLIP MCM30Ethicon Endo-Surgery, LLC · Applier, surgical, clip1 death236 reports
- WECK IPN915189Teleflex Incorporated · Applier, surgical, clip221 reports
- LIGACLIP MSM20Ethicon Endo-Surgery, LLC · Applier, surgical, clip152 reports
- LIGACLIP LX107Ethicon Endo-Surgery, LLC · Applier, surgical, clip105 reports
- WECK IPN028280Teleflex Incorporated · Applier, surgical, clip93 reports
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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