Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K042007 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Zoll E Series BLS Defibrillator/Pacemaker/Monitor Software versions 7.10 and 7.11 The product is... | 2 | 05/25/2011 | ZOLL Medical Corporation |
ZOLL E Series Defibrillator/Pacemaker/Monitors, BLS Model, with software versions 4.XX, 6.XX and 7.0... | 2 | 05/07/2010 | ZOLL Medical Corporation, World Wide Headquarters |
Zoll E Series Defibrillator with 12 Lead ECG, Automated external defibrillator, Software Version 3.0... | 2 | 06/28/2008 | ZOLL Medical Corporation, World Wide Headquarters |
-