Medical Device Recalls
-
1 result found
510(K) Number: K961008 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
AUTOMIX 3+3 Compounder with Accusource Monitoring System, product 2M8287; automated nutrition compou... | 2 | 02/22/2011 | Baxter Healthcare Corp. |
-