Medical Device Recalls
-
|
1 result found
510(K) Number: K012584 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Destination Guiding Sheath catheter introducer, Catalog Number: RSR06 Product Usage: The Destina... | 2 | 02/26/2018 | Terumo Medical Corporation |
-







