Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0608-2020 - HeartStart XL+ Defibrillator/Monitor, Model 861290 | 2 | 12/05/2019 |
FEI # 1218950 Philips North America, LLC |
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