Alcon Laboratories, Inc. / Huntington
FDA adverse event reports naming Alcon Laboratories, Inc. / Huntington as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON LABORATORIES, INC. / HUNTINGTON.
- Total reports
- 1,658
- Deaths
- 0
- Injuries
- 690
- Malfunctions
- 658
Reports per year
33200
56501
13702
9703
9404
9905
13306
20107
Source: FDA adverse event reports by year received, 2000–2007. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
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Recent recalls
No recalls listed in the FDA device recall database for this entry.
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