ArmadaRecalls & reported problems across all models
Abbott Vascular Inc. · 213 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Armada models — page 3
213 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Armada 1013463-100Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013463-120Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013464-120Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013464-150Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013466-020Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013466-080Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013466-120Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013466-150Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013468-080Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013469-060Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013469-080Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013470-020Catheter, angioplasty, peripheral, transluminal1 report
- Armada 1013470-180Catheter, angioplasty, peripheral, transluminal1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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