Sorin Group Italia SRL - CRF
6 FDA 510(k) clearances · Recalling firm
◉ Watch Sorin Group Italia SRL - CRF
| Record | Firm | Date |
|---|---|---|
| Platinium VR 1210, Model Number TDF031U, UDI/GTIN 08031527015514, Implantable cardioverter recall (Z-3228-2017) | Sorin Group Italia SRL - CRF | 2017-09-28 |
| Platinium DR 1510, Model Number TDF032U, UDI/GTIN 08031527015521, Implantable cardioverter recall (Z-3229-2017) | Sorin Group Italia SRL - CRF | 2017-09-28 |
| Platinium CRT DF1 1711, Model Number TDF033U, UDI/GTIN 08031527015538, Implantable cardiov recall (Z-3230-2017) | Sorin Group Italia SRL - CRF | 2017-09-28 |
| Platinium VR DF4 1240, Model Number TDF035U, UDI/GTIN 08031527015460, Implantable cardiove recall (Z-3231-2017) | Sorin Group Italia SRL - CRF | 2017-09-28 |
| Platinium DR DF4 1540, Model Number TDF036U, UDI/GTIN 08031527015477, Implantable cardiove recall (Z-3232-2017) | Sorin Group Italia SRL - CRF | 2017-09-28 |
| Platinium CRT-D 1741, Model Number TDF037U, UDI/GTIN 08031527015484, Implantable cardiover recall (Z-3233-2017) | Sorin Group Italia SRL - CRF | 2017-09-28 |
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Every clearance here is in the API, with alerts when new ones post.