Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K121674 |
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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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Aspire HD Plus, Aspire HD-s (for FDR-2000AWS) The Fujifilm Digital Mammography Systems, Aspire H... | 2 | 02/20/2018 | Fujifilm Medical Systems U.S.A., Inc. |
Aspire HD Plus (FDR MS-2500), also known as Aspire HD Plus F and Aspire HD-s (FDR MS-2000), also ... | 2 | 01/17/2018 | Fujifilm Medical Systems U.S.A., Inc. |
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