ORGClass 2
Platelet And Plasma Separator For Bone Graft Handling
FDA adverse event reports and recall history for platelet and plasma separator for bone graft handling (product code ORG), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 432
- Deaths
- 0
- Injuries
- 71
- Malfunctions
- 359
Reports per year
113
114
215
616
317
1018
1119
2020
2521
2522
8323
11724
10625
2226
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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