Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K861985 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended to be used in the anastom... | 2 | 04/08/2020 |
FEI # 1417572 Baxter Healthcare Corporation |
| GEM Microvascular Anastomotic Coupler Devices s intended to be used in the anastomosis of veins and ... | 2 | 04/08/2020 |
FEI # 1417572 Baxter Healthcare Corporation |
| GEM Microvascular Anastomotic Coupler Devices - Product Usage: s intended to be used in the anastomo... | 2 | 04/08/2020 |
FEI # 1417572 Baxter Healthcare Corporation |
-







