Medical Device Recalls
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1 to 5 of 5 Results
Recall Date to: 04/18/2015 510(K) Number: K040904 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs). Product Usage... | 2 | 03/19/2014 | Philips Medical Systems North America Inc. |
Automated External Defibrillator (AED) of brand name "Philips HeartStart HS1 Home" (Model Number M5... | 2 | 06/28/2010 | Philips Medical Systems |
Heartstart HS1 Defibrillator Model M5068A | 2 | 03/23/2010 | Philips Medical Systems |
Philips "HeartStart Home" defibrillator, model M5068A and is sold in the US over the counter. The ... | 2 | 07/09/2008 | Philips Medical Systems |
Philips defibrillator, model M5066A. Sold in the US by Philips as an OTC under the brand name Phili... | 2 | 07/09/2008 | Philips Medical Systems |
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