Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K932301 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Baxter Interlink System Y-Type Blood/Solution Set with 40 and 150 Micron Dual Screen Filter, Length ... | 2 | 01/11/2012 | Baxter Healthcare Corp. |
Baxter Interlink System Straight Type Blood Set with 40 and 150 Micron Dual Screen Filter, Length 86... | 2 | 01/11/2012 | Baxter Healthcare Corp. |
-