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/AEMS 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 during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor orthopaedic surgical planning and instrument guides automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.