Arizona Device Manufacturing
FDA adverse event reports naming Arizona Device Manufacturing as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ARIZONA DEVICE MANUFACTURING.
- Total reports
- 1,451
- Deaths
- 2
- Injuries
- 40
- Malfunctions
- 1,401
Reports per year
205
406
48207
84708
11409
110
111
Source: FDA adverse event reports by year received, 2005–2011. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Electrode, Ph, StomachFFT1,422
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW21
- Camera, Still, SurgicalFTT2
- Implantable Cardioverter Defibrillator (Non-Crt)LWS2
- Stimulator, Electrical, Implantable, For IncontinenceEZW1
- Stimulator, Spinal-Cord, Implanted (Pain Relief)GZB1
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS1
- Stimulator, Electrical, Implanted, For Parkinsonian TremorMHY1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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