SterlingRecalls & reported problems across all models
Boston Scientific Corporation · 153 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Sterling models — page 2
153 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Sterling™ H74939032702010CATHETER, PERCUTANEOUS3 reports
- Sterling™ H74939032806010CATHETER, PERCUTANEOUS3 reports
- Sterling™ H74939031452010CATHETER, PERCUTANEOUS3 reports
- Sterling™ H74939032501210Catheter, angioplasty, peripheral, transluminal3 reports
- Sterling™ H74939031601510Catheter, angioplasty, peripheral, transluminal3 reports
- Sterling™ H74939031701510Catheter, angioplasty, peripheral, transluminal3 reports
- Sterling™ H74939032200610Catheter, angioplasty, peripheral, transluminal3 reports
- Sterling™ H74939032408080CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939032602010CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939032608010CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939032702040CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939032802010CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939031552010CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939031352010CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939031554010CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939031703010CATHETER, PERCUTANEOUS2 reports
- Sterling™ H74939032501590Catheter, angioplasty, peripheral, transluminal2 reports
- Sterling™ H74939032502290Catheter, angioplasty, peripheral, transluminal2 reports
- Sterling™ H74939032602290Catheter, angioplasty, peripheral, transluminal2 reports
- Sterling™ H74939032702110Catheter, angioplasty, peripheral, transluminal2 reports
- Sterling™ H74939032300290Catheter, angioplasty, peripheral, transluminal2 reports
- Sterling™ H74939031515020Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032508080CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032108010CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032406080CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032701010CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032706010CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032708010CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032802040CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032803080CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032806080CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032808010CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939031402080CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939031403080CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939031501580CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939031554080CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939031703080CATHETER, PERCUTANEOUS1 report
- Sterling™ H74939032501290Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032502090Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032701210Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032702290Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939031302210Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939031402210Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032200490Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032202290Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032250490Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032250610Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032250690Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032252290Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032300210Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032350410Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032352210Catheter, angioplasty, peripheral, transluminal1 report
- Sterling™ H74939032402290Catheter, 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.
How reports and recalls are matched · Editorial policy · Report an error on this page