Medical Device Recalls
-
|
1 to 3 of 3 Results
510(K) Number: K030265 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Product 22 consists of all product under product code: JDI and same usage: Item no: 811400218 C... | 2 | 03/12/2016 |
FEI # 1000132037 Zimmer Manufacturing B.V. |
| CPT 12/14 COCR prosthesis, hip, semi-constrained, metal/polymer, porous uncemented various sizes ... | 2 | 02/22/2016 |
FEI # 1000220733 Zimmer Biomet, Inc. |
| CPT 12/14 COCR (various sizes) | 2 | 02/20/2014 |
FEI # 1000220733 Zimmer, Inc. |
-







