Medical Device Recalls
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1 to 10 of 12 Results
PMA Number: P030005 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
VISIONIST X4 CRT-P Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
VISIONIST CRT-P pacemaker, Models: a) U225 b) U226 c) U228 | 2 | 07/02/2021 | Boston Scientific Corporation |
VISIONIST CRT-P Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
VISIONIST X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) | 2 | 09/27/2018 | Boston Scientific Corporation |
VALITUDE X4 CRT-P Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
VALITUDE CRT-P pacemaker, Models: a) U125 b) U128 | 2 | 07/02/2021 | Boston Scientific Corporation |
VALITUDE CRT-P Pacemaker | 2 | 01/15/2018 | Boston Scientific Corporation |
VALITUDE X4 CRT-P (Cardiac Resynchronization Therapy Pacemaker) | 2 | 09/27/2018 | Boston Scientific Corporation |
INVIVE CRT-P, Model Numbers: a) V172 b) V173 c) V182 d) V183 e) W172 f) W173 | 1 | 07/13/2021 | Boston Scientific Corporation |
INTUA CRT-P, Model Numbers: a) V272 b) V273 c) W273 | 1 | 07/13/2021 | Boston Scientific Corporation |
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