Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K063375 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Philips HeartStart MRx devices in use with the M3539A AC Power Module: M3535A, M3536A, M3536M, M353... | 2 | 07/05/2019 | Philips North America, LLC |
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