Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K083533 |
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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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Hitachi Echelon MRI System | 2 | 03/23/2017 | Hitachi Medical Systems America Inc |
ECHELON MRI System | 2 | 08/24/2021 | Hitachi Healthcare Americas Corporation |
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