Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K061707 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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MRx Defibrillator Model # M3535A & M3536A, UDI 00884838000018(21)US00601969 Product Usage: The H... | 1 | 02/08/2018 | Philips North America, LLC |
HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M... | 1 | 03/24/2017 | Philips North America, LLC |
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