Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K020715 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Laerdal "HeartStart Defibrillator", model M5067A, under Laerdal brand for Laerdal Medical Corp, Wapp... | 2 | 07/09/2008 | Philips Medical Systems |
Philips HeartStart (HS1) Onsite/Home AED | 2 | 05/23/2018 | Philips Electronics North America Corp. |
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