Endoilluminator
FDA adverse event reports and recall history for endoilluminator (product code MPA), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 269
- Deaths
- 0
- Injuries
- 83
- Malfunctions
- 186
Reports per year
Source: FDA adverse event reports by year received, 2009–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
- 2025-10-24Open, ClassifiedProcess control
Brand Name: Alcon Laboratories, Inc. Product Name: Accessory devices for Unity and Constellation surgical consoles Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' 8065000252 UNITY 27 GA CHANDELIER 8065000253 UNITY 27+DS WIDE ANGLE LIGHT PROBE Software Version: N/A Product Description: These products are standalone accessory devices meant for vitrectomy surgical procedures. They interface with a corresponding Alcon surgical console. Component: N/A
Due to incomplete seals in the pouch which provide the sterile barrier.
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