Medical Device Recalls
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31 to 36 of 36 Results
Recall Date to: 07/05/2015 PMA Number: P910023 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Atlas DR, Models V-240 | 2 | 11/16/2005 | St Jude Medical |
Atlas VR, Models V-199 | 2 | 11/16/2005 | St Jude Medical |
Photo Micro VR/DR Models V-194 | 2 | 11/16/2005 | St Jude Medical |
Photo DR, Model V-230HV Implantable Cardioverter Defibrillator | 2 | 11/16/2005 | St Jude Medical |
Implantable Cardioverter Defibrilators Epic DR/HF (V-233/V-337/V-338), Epic Plus DR/VR/HF (V-236/... | 2 | 07/19/2005 | St Jude Medical |
Implantable Cardioverter-Defibrillator Models affected include the following: Atlas+ Models V-... | 2 | 04/13/2005 | St Jude Medical |
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