Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K050004 |
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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 FRx AED, Model 861304, FRx codeRev: E.02.017 | 2 | 02/19/2020 | Philips North America LLC |
Philips HeartStart HS1 Onsite (Model M5066A) and HSI Home (Model M5068A) AED, Model 861304, HSI code... | 2 | 02/19/2020 | Philips North America LLC |
Philips HeartStart FRx AED. | 2 | 05/23/2018 | Philips Electronics North America Corp. |
Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured by Philips Medical Syste... | 2 | 01/04/2013 | Philips Medical Systems North America Co. Phillips |
Philips HeartStart FRx Defibrillator, Automated External Defibrillator (AED), catalog number 861304.... | 3 | 11/22/2010 | Philips Medical Systems |
Automated External Defibrillator (AED) of brand name "Philips HeartStart FRx" (Model number 861304).... | 2 | 06/28/2010 | Philips Medical Systems |
Philips Heartstart FRx automated external defibrillator (AED), Model 861304 | 2 | 03/23/2010 | Philips Medical Systems |
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