Medical Device Recalls
-
1 result found
510(K) Number: K071263 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
NxStage Express Fluid Warmer (FW-300, FW-300-A, FW-300-WW, FW-301, FW-301-A) Product Usage: The ... | 2 | 08/14/2018 | NxStage Medical, Inc. |
-