FuseRecalls & reported problems across all models
Endochoice, Inc. · 11 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 30
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 0
We found 11 models of Fuse by Endochoice, Inc. in the FDA's device registry (GUDID). Together they are named in 30 adverse event reports in the FDA's MAUDE database, received between Aug 28, 2018 and Nov 11, 2019 — classified as 30 malfunctions.
The most frequently reported specific device problem is “Image Display Error/Artifact” (25 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Most reported Fuse problems
Device problems
- Image Display Error/Artifact25
- Poor Quality Image7
- Leak/Splash4
- Fogging1
Patient problems
- No Consequences Or Impact To Patient23
- No Known Impact Or Consequence To Patient7
Fuse models
11 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Fuse® FSC330-F7527Colonoscope And Accessories, Flexible/Rigid8 reports
- Fuse® FSC330-G7520Colonoscope And Accessories, Flexible/Rigid7 reports
- Fuse FSC-3300-150-RColonoscope And Accessories, Flexible/Rigid3 reports
- Fuse® FSC330-F7526Colonoscope And Accessories, Flexible/Rigid2 reports
- Fuse® FSC330-G7529Colonoscope And Accessories, Flexible/Rigid2 reports
- Fuse® FSC330-F7523Colonoscope And Accessories, Flexible/Rigid2 reports
- Fuse FSG250-H7641-RGastroscope And Accessories, Flexible/Rigid2 reports
- Fuse® FSG250-H7641Gastroscope And Accessories, Flexible/Rigid1 report
- Fuse FSC330-F7523-RColonoscope And Accessories, Flexible/Rigid1 report
- Fuse FSC330-G7529-RColonoscope And Accessories, Flexible/Rigid1 report
- Fuse FSC-3300-SL-RColonoscope And Accessories, Flexible/Rigid1 report
Recent Fuse adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionNov 11, 2019Image Display Error/Artifact; Poor Quality Image; Image Display Error/Artifact; Poor Quality Image
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38S SLIM COLONOSCOPE - R WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, ALL IMAGES IN THE SCOPE WERE PURPLE. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN THE ISSUE OCCURRED. ANOTHER FUSE C38S SLIM COLONOSCOPE - R WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9305628 ↗MalfunctionNov 7, 2019Image Display Error/Artifact; Poor Quality Image; Image Display Error/Artifact; Poor Quality Image
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE 1C COLONOSCOPE WAS DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE CENTER SCREEN WENT IN AND OUT. REPORTEDLY, THE IMAGES WERE INTERMITTENT ALL THROUGHOUT THE PROCEDURE. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN THESE ISSUES OCCURRED. THE PROCEDURE WAS COMPLETED WITH ANOTHER FUSE 1C COLONOSCOPE. 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 FINE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9289923 ↗MalfunctionNov 4, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38S SLIM COLONOSCOPE - S WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE IMAGES TURNED BLACK WHEN THE SCOPE WAS ANGULATED. THE ANATOMY OF THE PATIENT WAS NOT VISIBLE ON CENTER IMAGE WHEN THE ISSUE OCCURRED. ANOTHER FUSE C38S SLIM COLONOSCOPE - S WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9272141 ↗MalfunctionOct 23, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38S SLIM COLONOSCOPE - R WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, ONE OF THE IMAGES ON THE SCOPE WAS GREEN. THE ANATOMY OF THE PATIENT WAS NOT VISIBLE ON THE SCOPE WHEN THIS ISSUE OCCURRED. ANOTHER FUSE C38S SLIM COLONOSCOPE - R WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9226276 ↗MalfunctionApr 3, 2019Image Display Error/Artifact; Poor Quality Image; Image Display Error/Artifact; Poor Quality Image
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE 1C COLONOSCOPE WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON AN UNKNOWN DATE. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE MIDDLE CAMERA OF THE SCOPE WAS FLICKERING. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN IT WAS FLICKERING. ANTOHER FUSE 1C COLONOSCOPE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8478096 ↗MalfunctionApr 2, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38 COLONOSCOPE - R WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE CENTER IMAGE OF THE SCOPE WENT OUT WHEN THE SCOPE WAS ANGULATED BY THE PHYSICIAN. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN IT WENT OUT. THE CENTER IMAGE CAME BACK WHEN THE SCOPE WAS STRAIGHTEN OUT, THUS, COMPLETING THE PROCEDURE USING THE COMPLAINT DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8473945 ↗MalfunctionApr 2, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38S SLIM COLONOSCOPE - R WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE SCOPE HAD DARK IMAGES. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN THIS ISSUE OCCURRED. ANOTHER FUSE C38S SLIM COLONOSCOPE - R WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8473436 ↗MalfunctionMar 27, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE 1C COLONOSCOPE WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE CENTER IMAGE TURNED BLACK WHEN THE SCOPE WAS ANGULATED. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN IT TURNED BLACK. ANOTHER FUSE 1C COLONOSCOPE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8456985 ↗MalfunctionMar 21, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38 COLONOSCOPE - S WAS USED DURING A PROCEDURE PERFORMED ON AN UNKNOWN DATE. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE MIDDLE SCREEN OF THE SCOPE WENT OFF WHEN THE KNOB WAS TURNED. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN THE MIDDLE SCREEN WENT OFF. ANOTHER FUSE C38 COLONOSCOPE - S WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8439762 ↗MalfunctionMar 6, 2019Image Display Error/Artifact; Poor Quality Image; Image Display Error/Artifact; Poor Quality Image
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38S SLIM COLONOSCOPE - R WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE CENTER IMAGE FLICKERED WHEN THE SCOPE WAS ANGULATED. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN IT WAS FLICKERING. THE PROCEDURE WAS COMPLETED USING THE COMPLAINT DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8396374 ↗MalfunctionMar 5, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38S SLIM COLONOSCOPE - R WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON AN UNKNOWN DATE. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE SCOPE WHITED OUT. THE ANATOMY OF THE PATIENT WAS NOT VISIBLE WHEN THE SCOPE WHITED OUT. THE PROCEDURE WAS COMPLETED WITH ANOTHER FUSE C38S SLIM COLONOSCOPE- R. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8392248 ↗MalfunctionMar 4, 2019Fogging; Fogging
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38S SLIM COLONOSCOPE - R WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, WATER WAS NOTED IN THE FRONT LENS. THE PROCEDURE WAS COMPLETED USING THE COMPLAINT DEVICE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8387682 ↗MalfunctionFeb 19, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE C38S SLIM COLONOSCOPE -R WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, ALL IMAGES CHANGED COLOR DURING ANGULATION. THE ANATOMY OF THE PATIENT WAS NOT VISIBLE. ANOTHER FUSE C38S SLIM COLONOSCOPE -R WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8349383 ↗MalfunctionFeb 15, 2019Image Display Error/Artifact; Poor Quality Image; Image Display Error/Artifact; Poor Quality Image
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE 1C COLONOSCOPE WAS USED DURING A COLONOSCOPY PROCEDURE PERFORMED ON A UNKNOWN DATE. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE CENTER IMAGE FLICKERED, TURNED PINK THEN WENT BLACK. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN THE CENTER CAMERA WENT BLACK. ANOTHER FUSE 1C COLONOSCOPE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8343462 ↗MalfunctionFeb 5, 2019Image Display Error/Artifact; Image Display Error/Artifact
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A FUSE G28 GASTROSCOPE - R WAS USED DURING A GASTROSCOPY PROCEDURE PERFORMED ON (B)(6) 2019. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE CENTER IMAGE WAS BLURRY. THE PATIENT'S ANATOMY WAS NOT VISIBLE ON THE CENTER IMAGE WHEN IT WAS BLURRY. ANOTHER FUSE G28 GASTROSCOPE - R WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8306753 ↗
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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