Guidant Angleton/st. Paul
FDA adverse event reports naming Guidant Angleton/st. Paul as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: GUIDANT ANGLETON/ST. PAUL.
- Total reports
- 1,341
- Deaths
- 12
- Injuries
- 947
- Malfunctions
- 382
Reports per year
107
16709
22510
17211
12612
10213
9914
8315
13816
14917
7918
Source: FDA adverse event reports by year received, 2007–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Permanent Pacemaker ElectrodeDTB643
- Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker ElectrodesNVN511
- Implantable Pacemaker Pulse-GeneratorDXY69
- Implantable Cardioverter Defibrillator (Non-Crt)LWS40
- Pulse Generator, Permanent, ImplantableNVZ37
- Permanent Defibrillator ElectrodesNVY23
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP10
- Electrode, Pacing And Cardioversion, Temporary, EpicardialNHW3
- Pacemaker Lead AdaptorDTD2
- Catheter, Intravascular, DiagnosticDQO1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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