Angiomed Gmbh & Co. Medizintechnik Kg
FDA adverse event reports naming Angiomed Gmbh & Co. Medizintechnik Kg as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ANGIOMED GMBH & CO. MEDIZINTECHNIK KG.
- Total reports
- 5,014
- Deaths
- 59
- Injuries
- 1,298
- Malfunctions
- 3,656
Reports per year
18912
13213
14814
25415
33416
31917
25018
27919
38120
69721
39322
44023
47324
40125
15026
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
- Stent, Superficial Femoral ArteryNIP1,972
- System, Endovascular Graft, Arteriovenous (Av) Dialysis Access Circuit Stenosis TreatmentPFV1,475
- Stent, Iliac VeinQAN590
- Stent, IliacNIO557
- Stents, Drains And Dilators For The Biliary DuctsFGE254
- Prosthesis, Tracheal, ExpandableJCT109
- Needle, Aspiration And Injection, DisposableGAA21
- Needle, Biopsy, CardiovascularDWO14
- Instrument, BiopsyKNW7
- Stent, UreteralFAD4
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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