Medical Device Recalls
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1 result found
510(K) Number: K143538 |
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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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Angiographic Injector and Syringe, MEDRAD MRXperion MR Injection System, MEDRAD MRXperion Sterile Di... | 2 | 07/19/2016 | Bayer Healthcare |
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