|
Product Description
|
Recall Class
|
FDA Recall Posting Date
|
Recalling Firm
|
The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-...
|
2
|
11/16/2018
|
Boston Scientific Corporation
|
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse ...
|
2
|
09/13/2019
|
Boston Scientific Corporation
|
Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEM MRI S-ICD Puls...
|
2
|
09/13/2019
|
Boston Scientific Corporation
|
SQ-RX 1010 Pulse Generator, Rx.
Product Usage:
The S-ICD system is intended to provide defibril...
|
2
|
08/16/2017
|
Boston Scientific Corporation
|
EMBLEM S-ICD, Subcutaneous Implantable Defibrillators, Model A209, sterile.
|
2
|
10/31/2022
|
Boston Scientific Corporation
|
EMBLEM S-ICD, Model A209, Subcutaneous Implantable Cardioverter Defibrillator, RX.
Product Usag...
|
2
|
08/16/2017
|
Boston Scientific Corporation
|
EMBLEM S-ICD pulse generators, as part of Boston Scientific S-ICD System; Model A209
|
2
|
02/18/2021
|
Boston Scientific Corporation
|
EMBLEM S-ICD Subcutaneous Electrode Model 3501. Component of implantable cardioverter defibrillator...
|
1
|
01/19/2021
|
Boston Scientific Corporation
|
EMBLEM S-ICD Pulse Generator Model A209; Subcutaneous Implantable Cardioverter Defibrillator
|
2
|
08/22/2023
|
Boston Scientific Corporation
|
EMBLEM S-ICD Model A209
|
1
|
02/05/2021
|
Boston Scientific Corporation
|