Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K031187 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Philips Switched Internal Defibrillator Paddles (used with Philips HeartStart XL and HeartStart MRx ... | 2 | 03/15/2010 | Philips Healthcare Inc. |
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