TELEFLEX IPN921001Recalls & reported problems
Teleflex Incorporated · Large Clips - 1 Cartridge/1 Pouch · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 14026704737441), received between Dec 7, 2022 and Dec 7, 2022 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Difficult to Open or Close” (4 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
- Difficult to Open or Close4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 7, 2022Difficult to Open or Close; Difficult to Open or Close
REPORTED ISSUE: UROLOGIST WAS USING THE VESOLOCK IN A ROBOTIC PROSTATECTOMY AND CLIPS WOULD NOT LOCK. THREE PACKS OF CARTRIDGES OPENED AND ATTEMPTED BUT THERE WAS THE SAME PROBLEM WITH ALL PACKS. HEM-O-LOC FOUND AND USED SUCCESSFULLY AS A RESULT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15934101 ↗MalfunctionDec 7, 2022Difficult to Open or Close; Difficult to Open or Close
REPORTED ISSUE: UROLOGIST WAS USING THE VESOLOCK IN A ROBOTIC PROSTATECTOMY AND CLIPS WOULD NOT LOCK. THREE PACKS OF CARTRIDGES OPENED AND ATTEMPTED BUT THERE WAS THE SAME PROBLEM WITH ALL PACKS. HEM-O-LOC FOUND AND USED SUCCESSFULLY AS A RESULT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15934093 ↗MalfunctionDec 7, 2022Difficult to Open or Close; Difficult to Open or Close
REPORTED ISSUE: UROLOGIST WAS USING THE VESOLOCK IN A ROBOTIC PROSTATECTOMY AND CLIPS WOULD NOT LOCK. THREE PACKS OF CARTRIDGES OPE NED AND ATTEMPTED BUT THERE WAS THE SAME PROBLEM WITH ALL PACKS. HEM-O-LOC FOUND AND USED SUCCESSFULLY AS A RESULT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15933958 ↗MalfunctionDec 7, 2022Difficult to Open or Close; Difficult to Open or Close
REPORTED ISSUE: UROLOGIST WAS IN USE OF THE VESOLOCK IN A ROBOTIC PROSTATECTOMY AND CLIPS WOULD NOT LOCK. THREE PACKS OF CARTRIDGES OPENED AND ATTEMPTED BUT THERE WAS THE SAME PROBLEM WITH ALL PACKS. HEM-O-LOC FOUND AND USED SUCCESSFULLY AS A RESULT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15933916 ↗
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- Endo Clip III 176630Covidien LP · CLIP, IMPLANTABLE1 death1,959 reports
- Epix® Universal Clip Applier CA500Applied Medical Resources Corporation · Clip, Implantable1 recall1 death1,183 reports
- Endo Clip II 176657Covidien LP · CLIP, IMPLANTABLE1,183 reports
- LIGACLIP ER320Ethicon Endo-Surgery, LLC · CLIP, IMPLANTABLE1,115 reports
- Direct Drive® Clip Applier CA090Applied Medical Resources Corporation · Clip, Implantable1 death806 reports
- LAPRA-TY XC200Ethicon Inc. · CLIP, IMPLANTABLE791 reports
- Endo Clip 176625Covidien LP · CLIP, IMPLANTABLE1 death768 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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