Medical Device Recalls
-
|
1 result found
Recall Number: Z-0833-2016 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| NexGen Knee CR Porous FEM NexGen Knee CR Precoat FEM prosthesis, knee, patellofemorotibial, semi-c... | 2 | 02/22/2016 |
FEI # 1000220733 Zimmer Biomet, Inc. |
-







