Recall Z-0078-2018 ยท LWS Implantable Cardioverter Defibrillator (Non-Crt)
Boston Scientific Corporation
RESONATE EL ICD DR, Model D433, Sterile.
| Date | Oct 4, 2017 |
| Status | Terminated |
| Reason | The devices have an incorrect firmware configuration. |
| Root cause | Under Investigation by firm |
| Action | The recalling firm issued letters dated October 2017 on 10/4/2017 via delivery by the sales representative. |
| Quantity | 12 devices |
| Distribution | The devices were distributed to medical facilities located in MN and OH. There was no foreign/government/military distribution. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.