TELIGEN 286006061SRecalls & reported problems
Depuy Spine, LLC · TELIGEN VUE CAMERA · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034604510), received between Jan 6, 2026 and Feb 19, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Poor Quality Image” (2 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.
Reports received per month
Most reported problems
Device problems
- Poor Quality Image2
- Appropriate Device Problem Term/Code Not Available1
- Visual Prompts will not Clear1
Patient problems
- Cerebrospinal Fluid Leakage1
- Nerve Damage1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 19, 2026Poor Quality Image; Visual Prompts will not Clear
IT WAS REPORTED THAT THE IMAGE LOOKED LIKE A KALEIDOSCOPE WHEN THE CAMERA WAS PLUGGED IN. THEY REPLACED THE CAMERA, BUT THE IMAGE REMAINED THE SAME. THEY CHECKED ALL THE CONNECTIONS AND CHANGED THE IMAGE SETTINGS BACK TO DEFAULT BUT THE IMAGE REMAINED UNUSABLE. THEY TRANSITIONED TO X-RAY TO COMPLETE THE SURGERY. THE ISSUE WAS OBSERVED DURING SURGERY. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24393548 ↗InjuryJan 6, 2026Poor Quality Image; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT DURING A CASE, THE SURGEON COULD NOT DIFFERENTIATE BETWEEN TISSUE TYPES DUE TO POOR IMAGE QUALITY WHICH CAUSED AN INJURY TO THE PATIENT. A NERVE ROOT WAS DAMAGED CAUSING A CEREBRAL SPINAL FLUID (CSF) LEAK WHICH THE SURGEON HAD TO REPAIR BY PATCHING THE DAMAGED ROOT AND USING DURASEAL. THERE WAS PATIENT TREATMENT DELAY OR CANCELLATION. IT WAS REPORTED THAT THERE WAS NO FURTHER INFORMATION REGARDING THE ISSUE.
Patient problems: Cerebrospinal Fluid Leakage; Nerve Damage
MAUDE report 23981773 ↗
Other Arthroscope devices
- FMS 283512Medos International Sàrl · ARTHROSCOPE1,800 reports
- Arthrex® AR-6480Arthrex, Inc. · ARTHROSCOPE949 reports
- FMS VUE 284002Depuy Mitek, LLC · ARTHROSCOPE829 reports
- MITEK 242018Medos International Sàrl · Arthroscope731 reports
- METRx® System 9560100Medtronic Sofamor Danek, Inc. · Arthroscope667 reports
- FMS VUE II 284004Medos International Sàrl · Arthroscope562 reports
- VAPR COOLPULSE 228146Depuy Mitek, LLC · ARTHROSCOPE474 reports
- FMS DUO 284580Depuy Mitek, LLC · ARTHROSCOPE458 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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