Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K952684 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Nuclear Gamma Cameras (ADAC Vertex Classic, ADAC VERTEX PLUS/SOLUS/CARDIO, ADAC VERTEX V60) Philips ... | 2 | 05/12/2015 | Philips Medical Systems (Cleveland) Inc |
Nuclear gamma cameras (ADAC Vertex Plus, ADAC Solus, ADAC Vertex V60 & ADAC Vertex Classic) Philips ... | 2 | 04/26/2014 | Philips Medical Systems (Cleveland) Inc |
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