Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K112432 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Ver... | 2 | 03/31/2014 | ZOLL Medical Corporation |
Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is used by qualified me... | 2 | 09/17/2012 | ZOLL Medical Corporation |
-