MDT Powered Surgical Solutions
FDA adverse event reports naming MDT Powered Surgical Solutions as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MDT POWERED SURGICAL SOLUTIONS.
- Total reports
- 9,267
- Deaths
- 1
- Injuries
- 389
- Malfunctions
- 8,877
Reports per year
11712
7013
6014
6415
4916
3117
5918
10719
12020
29521
27722
31423
1,23624
2,37125
3,91126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Drills, Burrs, Trephines & Accessories (Simple, Powered)HBE5,156
- Motor, Drill, PneumaticHBB3,023
- Motor, Drill, ElectricHBC832
- Drill, Surgical, Ent (Electric Or Pneumatic) Including HandpieceERL192
- Drills, Burrs, Trephines & Accessories (Compound, Powered)HBF26
- Neurological Stereotaxic InstrumentHAW21
- Bur, Ear, Nose And ThroatEQJ7
- Bone MillLYS5
- Orthopedic Stereotaxic InstrumentOLO2
- Stimulator, NerveETN1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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