NA 242276Recalls & reported problems

Summary

The FDA's MAUDE database contains 23 adverse event reports that list this exact device (DI 10886705032143), received between Mar 29, 2022 and Sep 25, 2026 — classified as 23 malfunctions.

The most frequently reported specific device problem is “Display or Visual Feedback Problem” (13 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

Recent adverse event reports

The 23 most recent of 23 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 25, 2026Display or Visual Feedback Problem

  It was reported that the HD C-MNT SCP, 2.7, 30, 75, MITEK device appeared dingy in the picture. There was no patient involvement. There were no reports of injuries, medical intervention or prolonged hospitalization. All available information has been disclosed.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50899682 ↗
• MalfunctionSep 21, 2026Break; Crack

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50847307 ↗
• MalfunctionApr 29, 2026Material Fragmentation; Use of Device Problem

  IT WAS REPORTED THAT DURING AN ARTHROSCOPIC SCOPING PROCEDURE IT WAS OBSERVED THAT THE LENS OF THE HD C-MNT SCP,2.7,30,75,MITEK SCOPE DEVICE WAS DAMAGED. IT WAS REPORTED THAT THERE WAS A DELAY IN THE PROCEDURE DUE TO THE EVENT AND ANOTHER SAME DEVICE WAS USED, AND THE SURGERY WAS SUCCESSFULLY COMPLETED. DURING IN-HOUSE ENGINEERING EVALUATION IT WAS DETERMINED THAT THE DEVICE WAS BROKEN (2+ PIECES): CHIPPED/SHAVED/DELAMINATED. THERE WAS NO SURGICAL DELAY AND NO HARM TO THE PATIENT. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25028984 ↗
• MalfunctionDec 5, 2025Display or Visual Feedback Problem; Moisture Damage; Display or Visual Feedback Problem; Moisture Damage

  IT WAS REPORTED THAT THE HD C-MNT SCP, 2.7, 30, 75, MITEK DEVICE'S DEFECTIVE LENS CONTAINED WATER BUBBLES. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. THE EXACT DATE OF THE EVENT WAS UNKNOWN. HOWEVER, IT WAS REPORTED THAT THE EVENT OCCURRED IN 2025. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23728575 ↗
• MalfunctionSep 18, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem

  IT WAS REPORTED THAT DURING INSPECTION IT WAS OBSERVED THAT THE PICTURES OF 2X HD EPSCP,1.9,30,60,MITEK SCOPE DEVICES AND A HD C-MNT SCP,2.7,30,75,MITEK SCOPE DEVICE WERE BLOCKED/OUT OF FOCUS DURING TESTING. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WERE NO REPORTED ADVERSE CONSEQUENCES TO THE PATIENT. NO ADDITIONAL INFORMATION COULD BE PROVIDED. THIS IS REPORT 3 OF 3 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23082786 ↗
• MalfunctionSep 4, 2025Crack; Material Fragmentation; Crack; Material Fragmentation

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE, IT WAS DISCOVERED THAT THE SCOPE ON THE HD C-MNT SCP,2.7,30,75,MITEK DEVICE WAS CRACKED. THERE WERE NO DELAYS TO THE SURGICAL PROCEDURE. IT WAS NOT REPORTED IF A SPARE DEVICE WAS AVAILABLE FOR USE. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE DEVICE WAS BROKEN (2+ PIECES) : CHIPPED/SHAVED/DELAMINATED. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22965736 ↗
• MalfunctionAug 27, 2025Display or Visual Feedback Problem; Use of Device Problem; Display or Visual Feedback Problem; Use of Device Problem

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGERY, IT WAS OBSERVED THAT THE HD C-MNT SCP,2.7,30,75, MITEK DEVICE FOCUS RING WAS STICKING AND THE PICTURE ON THE SCREEN WAS GOING OUT OF FOCUS WHEN THE SURGEON SPUN THE LIGHT CORD. IT WAS REPORTED THAT THE SCOPE WAS SWAPPED OUT WITH A DIFFERENT LENS. THERE WAS A ONE TO MINUTE DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22901897 ↗
• MalfunctionJul 1, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE THE HD C-MNT SCP,2.7,30,75,MITEK DEVICE SCOPE WAS EXTREMELY BLURRY DESPITE BEING CLEANED MULTIPLE TIMES. ANOTHER DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22374782 ↗
• MalfunctionJun 4, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem

  IT WAS REPORTED THAT DURING INCOMING INSPECTION, IT WAS OBSERVED THAT THE SCOPE ON THE HD C-MNT SCP, 2.7,3 0, 75, MITEK DEVICE PRODUCED A CLOUDY IMAGE. THE EVENT WAS NOT RELATED TO SURGERY. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22144710 ↗
• MalfunctionMay 19, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem

  IT WAS REPORTED THAT DURING PRE-SURGERY FOR A WRIST ARTHROSCOPY SURGICAL PROCEDURE, IT WAS OBSERVED THAT THE HD C-MNT SCP,2.7,30,75, MITEK DEVICE SCOPE DID NOT TURN TO ADJUST THE FOCUS. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22043237 ↗
• MalfunctionMay 13, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem

  REPORT 2 OF 2 FOR (B)(4). IT WAS REPORTED THAT DURING INCOMING INSPECTION IT WAS OBSERVED THAT THE HD EPSCP,1.9,30,60, MITEK DEVICE SCOPE PRODUCED A CLOUDY IMAGE AND THE HD C-MNT SCP,2.7,30,75, MITEK DEVICE SCOPE ALSO PRODUCED A CLOUDY IMAGE. THIS EVENT DID NOT OCCUR DURING SURGERY. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22011225 ↗
• MalfunctionFeb 20, 2025Material Deformation; Material Deformation

  IT WAS REPORTED THAT DURING STERILIZATION, IT WAS OBSERVED THAT THE HD C-MNT SCP,2.7,30,75,MITEK DEVICE WAS FAULTY AND BENT. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE DEVICE WAS BROKEN (2+ PIECES): CHIPPED/SHAVED/DELAMINATED. THE EVENT WAS NOT RELATED TO SURGERY. THERE WAS NO PATIENT INVOLVEMENT REPORTED. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21421258 ↗
• MalfunctionJan 16, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem

  IT WAS REPORTED THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE, IT WAS DISCOVERED THAT VISIBILITY THROUGH THE HD C-MNT SCP, 2.7, 30, 75, MITEK DEVICE WAS NOT POSSIBLE. THERE WERE NO DELAYS TO THE SURGICAL PROCEDURE. IT WAS NOT REPORTED IF A SPARE DEVICE WAS AVAILABLE FOR USE. THERE WAS PATIENT INVOLVEMENT REPORTED. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21172415 ↗
• MalfunctionJul 15, 2024Display or Visual Feedback Problem; Use of Device Problem; Display or Visual Feedback Problem; Use of Device Problem

  IT WAS REPORTED THAT THE LENS ON THE HD C-MNT SCP,2.7,30,75,MITEK DEVICE SEEMED TO BE DAMAGED AS THE IMAGE WAS BLURRY AND FOGGY. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PROCEDURE NOR PATIENT INVOLVEMENT REPORTED. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19739392 ↗
• MalfunctionJun 20, 2024Break; Use of Device Problem; Break; Use of Device Problem

  IT WAS REPORTED BY THE SALES REP THAT AT THE START OF AN UNSPECIFIED SURGICAL PROCEDURE ON (B)(6) 2024, IT WAS OBSERVED THAT THE C-MOUNT ENDOSCOPE, MITEK LOCK 30 DEGREE X 2.7 MM X 75 MM DEVICE SCOPE WAS BROKEN. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE DEVICE WAS BROKEN (2+ PIECES: DEVICE FRACTURED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19573577 ↗
• MalfunctionMay 13, 2024Break; Appropriate Device Problem Term/Code Not Available; Break; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED BY THE SALES REP THAT DURING AN UNSPECIFIED SURGICAL PROCEDURE ON AN UNKNOWN DATE, IT WAS OBSERVED THAT WHILE USING THE FIXED FOCAL LENGTH COUPLER 19MM ALONG WITH THE C-MOUNT ENDOSCOPE, MITEK LOCK 30 DEGREE X 2.7 MM X 75 MM DEVICE THE MITEK LOCK HAD AN UNDETERMINED ISSUE. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE DEVICE WAS FRACTURED. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19296452 ↗
• MalfunctionMar 25, 2024Display or Visual Feedback Problem; Display or Visual Feedback Problem

  IT WAS REPORTED THAT PRIOR TO AN UNSPECIFIED SURGICAL PROCEDURE IT WAS OBSERVED THAT THE PICTURE OF THE HD C-MNT SCP,2.7,30,75,MITEK SCOPE WAS FUZZY, AND THE OBT_BUTTON_2.7,75_MITEK DEVICE WAS BENT AND THE SHE_2RSTCK_3.8,UNIV,75_MITEK SHEATH WAS BENT. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED. THIS IS REPORT 1 OF 2 FOR THE SAME EVENT IN (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18968007 ↗
• MalfunctionNov 22, 2023Fracture; Fracture

  IT WAS REPORTED BY THE SALES REP THAT THE HD C-MNT SCP,2.7,30,75,MITEK DEVICE SCOPE WAS NOT FUNCTIONAL. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE OPTICAL SYSTEM OPTICAL COMPONENTS HAD BROKEN LENSES. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18192184 ↗
• MalfunctionSep 11, 2023Break; Scratched Material; Break; Scratched Material

  IT WAS REPORTED BY THE SALES REP THAT DURING AN ANKLE ARTHROSCOPY ON (B)(6) 2023, IT WAS OBSERVED THAT THE HD C-MNT SCP,2.7,30,75,MITEK HAD MULTIPLE BLACK SCRATCHES FROM UNKNOWN SOURCE WHICH MADE THE DEVICE UNUSABLE. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE DEVICE WAS BROKEN/FRACTURED; AND HAD BROKEN LENSES IN ITS OPTICAL SYSTEM. IT WAS UNKNOWN IF AND HOW THE PROCEDURE WAS COMPLETED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17718514 ↗
• MalfunctionMay 19, 2023Break; Crack; Break; Crack

  IT WAS REPORTED BY THE SALES REP THAT DURING AN ANKLE RECONSTRUCTION PROCEDURE ON (B)(6) 2023, IT WAS OBSERVED THAT THE C-MOUNT ENDOSCOPE, MITEK LOCK 30 DEGREE X 2.7 MM X 75 MM DEVICE WAS DROPPED AND CRACKED. DURING IN-HOUSE ENGINEERING EVALUATION, IT WAS DETERMINED THAT THE OPTICAL PART ON THE DEVICE WAS BROKEN/FRACTURED. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES NOR SURGICAL DELAY REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16965348 ↗
• MalfunctionNov 1, 2022

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15710745 ↗
• MalfunctionJun 16, 2022Display or Visual Feedback Problem; Display or Visual Feedback Problem

  THIS IS REPORT 2 OF 4 FOR (B)(4). IT WAS REPORTED THROUGH IN-HOUSE DISTRIBUTION THAT DURING INSPECTION, IT WAS OBSERVED THAT FOUR ENDOSCOPE DEVICES HAVE FOGGY LENSES. THERE WAS NO PROCEDURE NOR PATIENT INVOLVEMENT REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14712550 ↗
• MalfunctionMar 29, 2022Display or Visual Feedback Problem; Display or Visual Feedback Problem

  IT WAS REPORTED BY THE SALES REP THAT DURING AN ANKLE SCOPE PROCEDURE ON (B)(6) 2022, IT WAS OBSERVED THAT THE CENTER ON THE C-MOUNT ENDOSCOPE, 30 DEGREE, 2.7 MM X 75 MM, MITEK LOCK ENDOSCOPE DEVICE APPEARED TO BE DAMAGED. ACCORDING TO THE REPORT, IT HAD A LINE ACROSS THE CENTER OF THE IMAGE WHICH WAS EXTREMELY NOTICEABLE WHEN LIGHT WAS REFLECTING ON THE SHAVER PIECE. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE WITH A MINIMAL UNSPECIFIED DELAY. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13942551 ↗