Resolution Clip M00522610Recalls & reported problems
Boston Scientific Corporation · Clipping Device · Class 2 · Implant
Quick summary
This Boston Scientific Resolution clip is a metal clip placed during endoscopy to stop bleeding in the digestive tract. Of its 1,118 reports, 12 describe injuries and 1,106 describe malfunctions, with no deaths. Most reports describe the clip failing to release or deploy, falling off the catheter, or activating early. In several reports, another device finished the procedure. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 1,116
- Deaths reported
- 0
- Injuries reported
- 12
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,116 adverse event reports that list this exact device (DI 08714729504795), received between Dec 9, 2016 and Aug 31, 2026 — classified as 12 injuries, 1,104 malfunctions.
The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (1,011 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
- Activation, Positioning or Separation Problem1,011
- Adverse Event Without Identified Device or Use Problem101
- Difficult to Open or Close94
- Use of Device Problem77
- Premature Activation73
- Material Deformation50
- Break45
- Device Contamination with Chemical or Other Material17
Patient problems
- No Clinical Signs, Symptoms or Conditions594
- No Consequences Or Impact To Patient460
- No Known Impact Or Consequence To Patient46
- Hemorrhage/Blood Loss/Bleeding19
- No Patient Involvement15
- Insufficient Information5
- Unspecified Tissue Injury3
- Discomfort2
Recent adverse event reports
The 25 most recent of 1,116 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 31, 2026Use of Device Problem; Activation, Positioning or Separation Problem; Human-Device Interface Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50533775 ↗MalfunctionJun 4, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT TWO RESOLUTION CLIPS WERE USED IN THE COLON DURING A COLON SCREENING PROCEDURE. DURING THE PROCEDURE, THE CLIP FAILED TO RELEASE FROM THE CATHETER. THE PROCEDURE WAS COMPLETED WITH AN ALTERNATIVE DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE FULLY RECOVERED. NOTE: THIS REPORT PERTAINS TO THE FIRST OF TWO DEVICES USED DURING THE SAME PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25391414 ↗MalfunctionJun 4, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT TWO RESOLUTION CLIPS WERE USED IN THE COLON DURING A COLON SCREENING PROCEDURE. DURING THE PROCEDURE, THE CLIP FAILED TO RELEASE FROM THE CATHETER. THE PROCEDURE WAS COMPLETED WITH AN ALTERNATIVE DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE FULLY RECOVERED. NOTE: THIS REPORT PERTAINS TO THE SECOND OF TWO DEVICES USED DURING THE SAME PROCEDURE. NO FURTHER INFORMATION HAS BEEN OBTAINED DESPITE GOOD FAITH EFFORTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25391412 ↗MalfunctionMay 18, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED IN THE ESOPHAGUS DURING A GASTROSCOPIC ESOPHAGEAL MUCOSAL DISSECTION PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP COULD NOT BE DEPLOYED WHILE IT WAS ENGAGED WITH THE TISSUE. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25208759 ↗MalfunctionApr 16, 2026Entrapment of Device; Human-Device Interface Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED IN THE COLON DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2026. IT WAS REPORTED THAT THE CLIP WOULD NOT DEPLOY THEN FELL OFF CATHETER WHILE REMOVING FROM SCOPE. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24904655 ↗MalfunctionMar 11, 2026Premature Activation
NOTE: THIS REPORT PERTAINS TO TWO OF THE FIVE RESOLUTION CLIPS THAT WERE USED IN THE SAME PROCEDURE. IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP DEVICE WAS USED FOR BLEEDING DURING AN ESOPHAGOGASTRODUODENOSCOPY (EGD) PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP FELL OFF BEFORE DEPLOYMENT STEPS WERE PERFORMED. THE PROCEDURE WAS COMPLETED WITH ANOTHER DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24567498 ↗MalfunctionMar 11, 2026Premature Activation
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED DURING AN EGD (ESOPHAGOGASTRODUODENOSCOPY) PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP PREMATURELY DEPLOYED IN UNKNOWN LOCATION. THE PROCEDURE WAS COMPLETED WITH AN ALTERNATIVE DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. NO FURTHER INFORMATION HAS BEEN OBTAINED DESPITE GOOD FAITH EFFORTS. NOTE: THIS REPORT PERTAINS TO FOUR OF FIVE CLIPS USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24567491 ↗MalfunctionMar 10, 2026Premature Activation
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED DURING AN EGD (ESOPHAGOGASTRODUODENOSCOPY) PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP PREMATURELY DEPLOYED IN UNKNOWN LOCATION. THE PROCEDURE WAS COMPLETED WITH AN ALTERNATIVE DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. NO FURTHER INFORMATION WAS OBTAINED DESPITE GOOD FAITH EFFORTS. NOTE: THIS REPORT PERTAINS TO FIVE OF FIVE CLIPS USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24561544 ↗MalfunctionMar 10, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED DURING A GASTROSCOPY PROCEDURE PERFORMED ON (B)(6) 2026. IT WAS REPORTED THAT THE CLIP UNABLE TO RELEASE FROM CATHETER. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. NO FURTHER INFORMATION HAS BEEN OBTAINED DESPITE GOOD FAITH EFFORTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24559680 ↗MalfunctionMar 6, 2026Premature Activation
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED DURING AN EGD (ESOPHAGOGASTRODUODENOSCOPY) PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP PREMATURELY DEPLOYED IN UNKNOWN LOCATION. THE PROCEDURE WAS COMPLETED WITH AN ALTERNATIVE DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. NO FURTHER INFORMATION WAS OBTAINED DESPITE GOOD FAITH EFFORTS. NOTE: THIS REPORT PERTAINS TO ONE OF FIVE CLIPS USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24531287 ↗MalfunctionMar 3, 2026Premature Activation
NOTE: THIS REPORT PERTAINS TO THE FIRST OF FIVE RESOLUTION CLIP USED DURING THE SAME PROCEDURE. IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED IN AN UNKNOWN ANATOMY DURING AN EGD (ESOPHAGOGASTRODUODENOSCOPY) PROCEDURE PERFORMED ON (B)(6) 2026. IT WAS REPORTED THAT THE CLIP WOULD DEPLOY BEFORE DEPLOYMENT STEPS WERE TAKEN. THE PROCEDURE WAS COMPLETED WITH ALTERNATIVE METHOD. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24500187 ↗MalfunctionMar 3, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED IN THE STOMACH FOR HEMOSTASIS DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP TIP OF THE HANDLE COULD NOT BE DEPLOYED AFTER BEING PUSHED AND PULLED FOR MANY TIMES. THE PROCEDURE WAS COMPLETED WITH ANOTHER OF THE SAME DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT, AND THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24496396 ↗MalfunctionMar 2, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED IN THE INTESTINAL TRACT DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) WOUND HEMOSTASIS PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP COULD NOT BE DEPLOYED PROPERLY. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24484144 ↗MalfunctionFeb 24, 2026Activation, Positioning or Separation Problem; Human-Device Interface Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) PROCEDURE PERFORMED ON (B)(6) 2026. IT WAS REPORTED THAT DURING THE PROCEDURE, THE RESOLUTION CLIP COULD NOT BE COMPLETELY DEPLOYED AFTER THE HANDLE WAS PUSHED AND PULLED FOR MANY TIMES. THE PROCEDURE WAS COMPLETED WITH ANOTHER OF THE SAME DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. ADDITIONAL INFORMATION WAS RECEIVED ON FEBRUARY 25, 2026, STATING THAT A POOR BITE OCCURRED, NOT FAILURE TO RELEASE FROM CATHETER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24428752 ↗MalfunctionFeb 20, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP DEVICE WAS USED FOR INTESTINAL POLYPS IN THE INTESTINAL TRACT DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) FOR A WOUND HEMOSTASIS PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP COULD NOT BE DEPLOYED PROPERLY. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24406222 ↗MalfunctionFeb 20, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP DEVICE WAS USED FOR INTESTINAL POLYPS IN THE INTESTINAL TRACT DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) FOR A WOUND HEMOSTASIS PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP WAS ABLE TO GRASP AND LOCK ONTO TISSUE; HOWEVER, THE CLIP COULD NOT DETACH FROM THE CATHETER TO DEPLOY. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24406211 ↗MalfunctionFeb 20, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP DEVICE WAS USED IN THE INTESTINAL TRACT DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) WOUND HEMOSTASIS PROCEDURE TO TREAT BLEEDING PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP COULD NOT BE DEPLOYED PROPERLY. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24400881 ↗MalfunctionFeb 11, 2026Activation, Positioning or Separation Problem; Human-Device Interface Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED IN THE STOMACH FUNDUS DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) PROCEDURE PERFORMED ON (B)(6) 2026. DURING THE PROCEDURE, THE CLIP COULD NOT BE DEPLOYED COMPLETELY. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE. ADDITIONAL INFORMATION RECEIVED ON FEBRUARY 12, 2025. IT WAS CLARIFIED THAT THE MAIN PROBLEM OF THE DEVICE WAS THE CLIP UNABLE TO GRASP ONTO TISSUE, THUS MAKING THIS A POOR BITE ISSUE NOT A DEPLOYMENT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24314906 ↗MalfunctionFeb 10, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP DEVICE WAS USED IN THE STOMACH DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) PROCEDURE TO TREAT EARLY STOMACH CANCER PERFORMED ON (B)(6) 2025. DURING THE PROCEDURE, THE CLIP COULD NOT BE DEPLOYED. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION CLIP DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24307286 ↗MalfunctionJan 27, 2026Activation, Positioning or Separation Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON UNKNOWN DATE. DURING THE PROCEDURE, THE CLIP FAILED TO DEPLOY. THE PROCEDURE WAS COMPLETED WITH ANOTHER OF THE SAME DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24191364 ↗MalfunctionJan 14, 2026Premature Activation; Activation, Positioning or Separation Problem; Difficult to Open or Close; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP DEVICE WAS USED DURING AN UNKNOWN PROCEDURE PERFORMED ON (B)(6) 2025. THE ANATOMICAL LOCATION IS UNKNOWN. DURING THE PROCEDURE, THE CLIP WOULD NOT OPEN. IT WAS NOTED THAT THE CLIP PREMATURELY DEPLOYED. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. NO FURTHER INFORMATION HAS BEEN OBTAINED DESPITE GOOD FAITH EFFORTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24068106 ↗MalfunctionJan 7, 2026Activation, Positioning or Separation Problem; Difficult to Advance
NOTE: NOTE: THIS REPORT PERTAINS TO ONE OF TWO DEVICES USED DURING THE SAME PROCEDURE. IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT TWO RESOLUTION CLIPS WERE USED DURING AN UNKNOWN PROCEDURE PERFORMED ON (B)(6) 2025. DURING THE PROCEDURE, IT WAS REPORTED THAT THE CLIPS FELT LIKE THEY WERE SNAGGING DURING INSERTING INTO SCOPE AND WOULD NOT DEPLOY BUT EVENTUALLY DEPLOYED CLOSED AND UNATTACHED. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION 360 CLIP. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23989040 ↗MalfunctionJan 7, 2026Activation, Positioning or Separation Problem; Difficult to Advance
NOTE: THIS REPORT PERTAINS TO ONE OF TWO DEVICES USED DURING THE SAME PROCEDURE. IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT TWO RESOLUTION CLIPS WERE USED DURING AN UNKNOWN PROCEDURE PERFORMED ON (B)(6) 2025. DURING THE PROCEDURE, IT WAS REPORTED THAT THE CLIPS FELT LIKE THEY WERE SNAGGING DURING INSERTING INTO SCOPE AND WOULD NOT DEPLOY BUT EVENTUALLY DEPLOYED CLOSED AND UNATTACHED. THE PROCEDURE WAS COMPLETED WITH ANOTHER RESOLUTION 360 CLIP. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23989021 ↗MalfunctionDec 19, 2025Premature Activation; Premature Activation
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP WAS USED DURING A GASTROSCOPIC TREATMENT PROCEDURE PERFORMED ON (B)(6) 2025. DURING THE PROCEDURE, THE CLIP PREMATURELY DEPLOYED IN THE ESOPHAGUS. THE PROCEDURE WAS COMPLETED WITH ANOTHER OF THE SAME DEVICE. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23856808 ↗MalfunctionDec 16, 2025Activation, Positioning or Separation Problem; Adverse Event Without Identified Device or Use Problem; Activation, Positioning or Separation Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESOLUTION CLIP DEVICE WAS USED IN THE STOMACH DURING AN ENDOSCOPIC SUBMUCOSAL DISSECTION (ESD) PROCEDURE FOR BLEEDING, PERFORMED ON (B)(6) 2025. DURING THE PROCEDURE, THE CLAMP HEAD OF THE HANDLE COULD NOT BE RELEASED AFTER BEING PUSHED AND PULLED MULTIPLE TIMES. THE PROCEDURE WAS COMPLETED USING ANOTHER RESOLUTION CLIP DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23817650 ↗
Other Hemostatic metal clip for the GI tract devices
- Resolution 360 Clip M00521230Boston Scientific Corporation · Hemostatic metal clip for the GI tract3 deaths2,291 reports
- Instinct G58010Cook Incorporated · Hemostatic metal clip for the GI tract1 recall1,017 reports
- Resolution 360™ ULTRA Clip M00521400Boston Scientific Corporation · Hemostatic metal clip for the GI tract3 deaths496 reports
- Instinct G18343Cook Incorporated · Hemostatic metal clip for the GI tract244 reports
- MANTIS™ Clip M00521420Boston Scientific Corporation · Hemostatic metal clip for the GI tract195 reports
- Single Use Repositionable Clip HX-202UROlympus Medical Systems Corp. · Hemostatic metal clip for the GI tract1 recall118 reports
- colonic FTRD Set 14Ovesco Endoscopy AG · Hemostatic Metal Clip For The Gi Tract2 deaths95 reports
- Single Use Repositionable Clip HX-202UROlympus Medical Systems Corp. · Hemostatic metal clip for the GI tract87 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.