Cordis LLC (pr)
FDA adverse event reports naming Cordis LLC (pr) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CORDIS LLC (PR).
- Total reports
- 5,760
- Deaths
- 533
- Injuries
- 4,148
- Malfunctions
- 1,038
Reports per year
71803
1,06704
75405
59506
38607
27708
23109
49010
52811
55012
11513
4914
Source: FDA adverse event reports by year received, 2003–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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