Medical Device Recalls
-
11 to 12 of 12 Results
510(K) Number: K020715 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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 |
-