EverCrossRecalls & reported problems across all models
Ev3, Inc · 114 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
EverCross models — page 2
114 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- EverCross™ AB35W06120080Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W07040135Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W07060135Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W07080135Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W07120135Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W07200135Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W08060135Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W09060080Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W10020080CATHETER, PERCUTANEOUS1 report
- EverCross™ AB35W10040135Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W10060080Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W10060135Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W12040080Catheter, angioplasty, peripheral, transluminal1 report
- EverCross™ AB35W12060135Catheter, 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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