Medical Device Recalls
-
1 to 3 of 3 Results
Related Medical Device Recalls |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Z-0944-2017 - Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have fa... | 2 | 01/04/2017 | Smith & Nephew, Inc. |
Z-0946-2017 - Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilita... | 2 | 01/04/2017 | Smith & Nephew, Inc. |
Z-0945-2017 - Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilit... | 2 | 01/04/2017 | Smith & Nephew, Inc. |
-