MUSTANGRecalls & reported problems across all models
Boston Scientific Corporation · 131 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
MUSTANG models — page 2
131 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- MUSTANG™ H74939171030410CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171071210CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171061270CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171090210CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171081210CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171041570Catheter, angioplasty, peripheral, transluminal2 reports
- MUSTANG™ H74939171090670CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171070840CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171061040CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171030810CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171030870CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171060840CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171090840CATHETER, BILIARY, DIAGNOSTIC2 reports
- MUSTANG™ H74939171070210CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171051270CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171030270CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171082010Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171081510Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171030210CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171082070Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171051810Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171070370CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171070240CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171100370CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171081270CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171081570Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171071810Catheter, angioplasty, peripheral, transluminal1 report
- MUSTANG™ H74939171100840CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171031070CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171050840CATHETER, BILIARY, DIAGNOSTIC1 report
- MUSTANG™ H74939171090640CATHETER, BILIARY, DIAGNOSTIC1 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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