Alcon Grieshaber Ag
FDA adverse event reports naming Alcon Grieshaber Ag as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON GRIESHABER AG.
- Total reports
- 1,456
- Deaths
- 0
- Injuries
- 355
- Malfunctions
- 1,101
Reports per year
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
- 2013-06-06TerminatedUse error
The Constellation Vision System Pneumatic Handpiece. Indicated for both anterior and posterior segment opthalmic surgery.
Alcon is conducting a Medical Device Removal for the Constellation Pneumatic Handpiece, DSP, product number 725.01. This action is being taken because the forceps or scissors tips (sold separately) may dislodge from the hand piece, if not attached by the user according to the Directions for Use.
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