Medical Device Recalls
-
|
1 result found
Related Medical Device Recalls |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Z-0037-2012 - LATITUDE® Paceart Integration Software, version 1.00 Model 6472. LATITUDE Paceart Integration is software and therefore does not have any serial numbers. However, the software version affected is ... | 2 | 10/12/2011 |
FEI # 2124215 Boston Scientific CRM Corp |
-







