Medical Device Recalls
-
|
1 result found
510(K) Number: K931549 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Alaris® SE Pump (formerly Signature Edition® Infusion Pump); Model Numbers: 7000, 7100, 7101, 7130, ... | 1 | 09/19/2006 | Cardinal Health 303 Inc DBA Alaris Products |
-







