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
- 2,462
- Deaths
- 0
- Injuries
- 1,135
- Malfunctions
- 1,004
Reports per year
25600
1,08901
29502
21303
19904
16005
11006
14007
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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