Balt USA LLC
514 devices · 309 adverse event reports · 5 deaths reported · 454 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- Barricade Coil System 900114Device, Neurovascular Embolization1 report
- Barricade Coil System 900116Device, Neurovascular Embolization1 report
- Barricade Coil System 900123Device, Neurovascular Embolization1 report
- Barricade Coil System 900128Device, Neurovascular Embolization1 report
- HYBRID Guidewire HYBRID008DWire, Guide, Catheter1 report
- Magic Infusion Catheter MA1.5FOLIVEMPCatheter, Continuous Flush1 report
- Ballast 088 Long Sheath BALLAST80Catheter, Percutaneous1 report
- Ballast 088 Long Sheath BALLAST100Catheter, Percutaneous1 report
- Optima Coil System OPTI0427BLKDevice, Neurovascular Embolization1 report
- Optima Coil System OPTI0212BLKTDevice, Vascular, For Promoting Embolization1 report
- Prestige Coil System PRESPACK30V02Device, Vascular, For Promoting Embolization1 report
- Optima Coil System OPTI0435BLKDevice, Vascular, For Promoting Embolization1 report
- Optima Coil System OPTI0650BLKDevice, Vascular, For Promoting Embolization1 report
- Optima Coil System OPTI1465BLKDevice, Neurovascular Embolization1 report