Medical Device Recalls
-
1 to 7 of 7 Results
Recall Date to: 04%2F17%2F2014 510(K) Number: K040904 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 |
Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs). Product Usage... | 2 | 03/19/2014 | Philips Medical Systems North America Inc. |
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, Model 861304, FRx codeRev: E.02.017 | 2 | 02/19/2020 | Philips North America LLC |
Philips "HeartStart Home" defibrillator, model M5068A and is sold in the US over the counter. The ... | 2 | 07/09/2008 | Philips Medical Systems |
Heartstart HS1 Defibrillator Model M5068A | 2 | 03/23/2010 | Philips Medical Systems |
Automated External Defibrillator (AED) of brand name "Philips HeartStart HS1 Home" (Model Number M5... | 2 | 06/28/2010 | Philips Medical Systems |
-