MI Product Line 061525Recalls & reported problems
Medical Illumination International Inc. · MI-1000 Minor Surgical Light, Dual Ceiling · Class 2
- 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 00816835020171), received between Jan 3, 2024 and Jan 3, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Integrity Problem” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Material Integrity Problem1
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.
MalfunctionJan 3, 2024Material Integrity Problem; Material Integrity Problem
ON NOVEMBER 30TH, IT WAS REPORTED TO MEDICAL ILLUMINATION THAT AN MI-1000 LIGHT SYSTEM HAD SEPARATED FROM THE DOWN TUB TO THE CEILING MOUNT. THE REPORTER ALSO STATED SOMEONE HAD RECEIVED STITCHES. WE WERE UNABLE TO CONFIM THIS DUE TO LOCATION (SEOUL, KOREA).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18439766 ↗
Other Light, Surgical, Fiberoptic devices
- NA 242386Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC49 reports
- Arthrex® AR-3240-5027Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC30 reports
- Integra® 001388LX9Integra Lifesciences (Ireland) Limited · LIGHT, SURGICAL, FIBEROPTIC7 reports
- N/A FC1SPStryker Corporation · Light, Surgical, Fiberoptic5 reports
- UltraLite® AX2100BIFIntegra Lifesciences (Ireland) Limited · LIGHT, SURGICAL, FIBEROPTIC4 reports
- NA 242387Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC3 reports
- Arthrex® AR-3240-5040Arthrex, Inc. · LIGHT, SURGICAL, FIBEROPTIC3 reports
- NA 242388Medos International Sàrl · LIGHT, SURGICAL, FIBEROPTIC2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.