Perclose, Inc.
FDA adverse event reports naming Perclose, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: PERCLOSE, INC..
- Total reports
- 1,786
- Deaths
- 56
- Injuries
- 1,357
- Malfunctions
- 348
Reports per year
6897
13498
28299
22600
24701
20702
28003
19804
13605
806
Source: FDA adverse event reports by year received, 1997–2006. 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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