Medical Device Recalls
-
|
1 to 4 of 4 Results
510(K) Number: K121393 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| LEGION AP Cutting Block Size 4, REF 71434409; LEGION AP Cutting Block Size 6, REF 71434411; LEGION... | 2 | 01/28/2020 |
FEI # 1020279 Smith & Nephew, Inc. |
| Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK, SIZE 6 REF 71434411, QTY: (1) ... | 2 | 10/22/2018 |
FEI # 1020279 Smith & Nephew, Inc. |
| smith&nephew GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1) | 2 | 06/11/2018 |
FEI # 1020279 Smith & Nephew, Inc. |
| smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING, REF CATALOG NUMBER 71440014 The GENESIS ... | 2 | 05/21/2018 |
FEI # 1020279 Smith & Nephew, Inc. |
-







