Genzyme Biosurgery (ridgefield)
FDA adverse event reports naming Genzyme Biosurgery (ridgefield) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: GENZYME BIOSURGERY (RIDGEFIELD).
- Total reports
- 3,306
- Deaths
- 20
- Injuries
- 1,387
- Malfunctions
- 482
Reports per year
207
14808
22309
24810
30211
32612
46113
20314
17415
17816
29717
72118
2319
Source: FDA adverse event reports by year received, 2007–2019. 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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