Medical Device Recalls
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61 to 61 of 61 Results
PMA Number: P910023 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Implantable Cardioverter-Defibrillator Models affected include the following: Atlas+ Models V-... | 2 | 04/13/2005 | St Jude Medical |
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