mi-tablet 2 T200-020Recalls & reported problems
Trice Medical, Inc. · Tablet for use as part of the mi-eye 2 System. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00857356008064), received between Jul 26, 2023 and Jul 26, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Melted” (1 report).
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.
Most reported problems
Device problems
- Melted1
- Overheating of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 26, 2023Melted; Overheating of Device; Melted; Overheating of Device
A FACILITY REPORTED THAT UPON SETTING UP THE DEVICE, WITH THE POWER CORD PLUGGED INTO THE WALL OUTLET AND INTO THE POWER SUPPLY, THE POWER CORD STARTED TO GET WARM AND GENERATE SMOKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17401845 ↗
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- 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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