PBFClass 2
Orthopaedic Surgical Planning And Instrument Guides
FDA adverse event reports and recall history for orthopaedic surgical planning and instrument guides (product code PBF), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 225
- Deaths
- 0
- Injuries
- 185
- Malfunctions
- 39
Reports per year
212
114
218
119
220
1221
5322
4523
3424
6225
1126
Source: FDA adverse event reports by year received, 2012–2026. 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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