TELEFLEX IPN921000Recalls & reported problems
Teleflex Incorporated · Medium Large Clips - 1 Cartridge/1 Pouch · Class 2 · Implant
- Adverse event reports
- 12
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 14026704737434), received between Nov 10, 2022 and Jul 12, 2023 — classified as 1 injury, 11 malfunctions.
The most frequently reported specific device problem is “Failure to Form Staple” (6 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.
Most reported problems
Device problems
- Failure to Form Staple6
- Break4
- Use of Device Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions11
- Foreign Body In Patient1
Recent adverse event reports
The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 12, 2023Use of Device Problem; Use of Device Problem
IT WAS REPORTED THAT WHILE IN USE ON A PATIENT DURING THE CLIPPING OF AN ARTERY, THE CLIP WOULD NOT CLIP INTO THE SECURED POSITION. AS A RESULT, A 2ND PACKAGE WAS OPENED AND USED AND THE SAME EVENT OCCURRED. THE ISSUE WAS RESOLVED BY USING DEVICE FROM A DIFFERENT BRAND. NO PATIENT HARM OR INJURY. ASSOCIATED MDR #3011137372-2023-00191.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17309601 ↗MalfunctionJul 12, 2023Use of Device Problem; Use of Device Problem
IT WAS REPORTED THAT WHILE IN USE ON A PATIENT DURING THE CLIPPING OF AN ARTERY, THE CLIP WOULD NOT CLIP INTO THE SECURED POSITION. AS A RESULT, A 2ND PACKAGE WAS OPENED AND USED AND THE SAME EVENT OCCURRED. THE ISSUE WAS RESOLVED BY USING DEVICE FROM A DIFFERENT BRAND. NO PATIENT HARM OR INJURY. SEE ASSOCIATED MDR #3011137372-2023-00182.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17309518 ↗MalfunctionJul 11, 2023Failure to Form Staple; Failure to Form Staple
IT WAS REPORTED THAT DURING A LAPAROSCOPIC CHOLECYSTECTOMY, "VESOLOCK CLIP WAS NOT DEPLOYING/CLIPPING DURING MULTIPLE PROCEDURES". AS A RESULT, "A DIFFERENT SIZED CLIP WAS USED" TO COMPLETE THE PROCEDURE. NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT STATUS IS REPORTED AS "DISCHARGED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17300031 ↗MalfunctionJul 11, 2023Failure to Form Staple; Failure to Form Staple
IT WAS REPORTED THAT DURING A LAPAROSCOPIC CHOLECYSTECTOMY, "VESOLOCK CLIP WAS NOT DEPLOYING/CLIPPING DURING MULTIPLE PROCEDURES". AS A RESULT, "A DIFFERENT SIZED CLIP WAS USED" TO COMPLETE THE PROCEDURE. NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT STATUS IS REPORTED AS "DISCHARGED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17299972 ↗MalfunctionJul 11, 2023Failure to Form Staple; Failure to Form Staple
IT WAS REPORTED THAT DURING A LAPAROSCOPIC CHOLECYSTECTOMY, "VESOLOCK CLIP WAS NOT DEPLOYING/CLIPPING DURING MULTIPLE PROCEDURES". AS A RESULT, "A DIFFERENT SIZED CLIP WAS USED" TO COMPLETE THE PROCEDURE. NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT STATUS IS REPORTED AS "DISCHARGED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17299610 ↗MalfunctionJul 11, 2023Failure to Form Staple; Failure to Form Staple
IT WAS REPORTED THAT DURING A LAPAROSCOPIC CHOLECYSTECTOMY, "VESOLOCK CLIP WAS NOT DEPLOYING/CLIPPING DURING MULTIPLE PROCEDURES". AS A RESULT, "A DIFFERENT SIZED CLIP WAS USED" TO COMPLETE THE PROCEDURE. NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT STATUS IS REPORTED AS "DISCHARGED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17299473 ↗MalfunctionJul 11, 2023Failure to Form Staple; Failure to Form Staple
IT WAS REPORTED THAT DURING A LAPAROSCOPIC CHOLECYSTECTOMY, "VESOLOCK CLIP WAS NOT DEPLOYING/CLIPPING DURING MULTIPLE PROCEDURES". AS A RESULT, "A DIFFERENT SIZED CLIP WAS USED" TO COMPLETE THE PROCEDURE. NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT STATUS IS REPORTED AS "DISCHARGED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17299372 ↗MalfunctionMay 30, 2023Failure to Form Staple; Failure to Form Staple
IT WAS REPORTED THAT WHILE IN USE ON A PATIENT DURING A NON-ROBOTIC LAPAROSCOPIC CHOLECYSTECTOMY, THE CLIPS DID NOT CLOSE PROPERLY. AS A RESULT, NEW CLIPS WERE USED TO SUCCESSFULLY COMPLETE THE PROCEDURE. NO PATIENT HARM OR INJURY. THE PATIENT STATUS IS REPORTED AS FINE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17020380 ↗MalfunctionApr 26, 2023Break; Break
REPORTED AS "WEAKNESS IN HINGE OF CLIP". IT WAS REPORTED THAT DURING USE ON A PATIENT, THE CLIP BROKE AT THE HINGE POINT WHEN ATTEMPTING TO CLIP A VESSEL OR DUCT. NO REPORT OF PATIENT HARM OR INJURY. PER THE CUSTOMER, IT IS UNKNOWN WHAT THE CURRENT STATUS OF THE PATIENT IS. IF FURTHER INFORMATION IS RECEIVED, THE COMPLAINT FILE WILL BE UPDATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16820113 ↗MalfunctionApr 26, 2023Break; Break
REPORTED AS "WEAKNESS IN HINGE OF CLIP". IT WAS REPORTED THAT DURING USE ON A PATIENT, THE CLIP BROKE AT THE HINGE POINT WHEN ATTEMPTING TO CLIP A VESSEL OR DUCT. NO REPORT OF PATIENT HARM OR INJURY. PER THE CUSTOMER, IT IS UNKNOWN WHAT THE CURRENT STATUS OF THE PATIENT IS. IF FURTHER INFORMATION IS RECEIVED, THE COMPLAINT FILE WILL BE UPDATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16820038 ↗MalfunctionApr 26, 2023Break; Break
REPORTED AS "WEAKNESS IN HINGE OF CLIP". IT WAS REPORTED THAT DURING USE ON A PATIENT, THE CLIP BROKE AT THE HINGE POINT WHEN ATTEMPTING TO CLIP A VESSEL OR DUCT. NO REPORT OF PATIENT HARM OR INJURY. PER THE CUSTOMER, IT IS UNKNOWN WHAT THE CURRENT STATUS OF THE PATIENT IS. IF FURTHER INFORMATION IS RECEIVED, THE COMPLAINT FILE WILL BE UPDATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16819950 ↗InjuryNov 10, 2022Break; Break
IT WAS REPORTED THAT A ML VESOLOCK CLIP BROKE DURING A ROBOTIC LAPAROSCOPY CHOLECYSTOMY CASE. ADDITIONAL INFORMATION: IT IS UNKNOWN IF ANY PART OF THE BROKEN CLIP FELL INSIDE THE PATIENT; NOTING WAS FOUND. THE CLIP WAS BEING APPLIED TO A VESSEL WHEN IT BROKE AND THERE WAS NO REPORTED VESSEL DAMAGE.
Patient problems: Foreign Body In Patient
MAUDE report 15775193 ↗
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- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.