Medical Device Recalls
-
1 to 5 of 5 Results
510(K) Number: K872379 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Product 51 consists of all product under product code: JWH and same usage: Item no: 598603701 NE... | 2 | 03/12/2016 | Zimmer Manufacturing B.V. |
Product 35 consists of all product under product code: JWH and same usage: Item no: 522007300 I... | 2 | 03/12/2016 | Zimmer Manufacturing B.V. |
I/B II KNEE DOMED PATELLA, I/B II KNEE FLUTED ROD (1 and 2), MGII KNEE 10MM PATELLA (2,3 and 4), MGI... | 2 | 02/20/2014 | Zimmer, Inc. |
MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFF... | 2 | 02/20/2014 | Zimmer, Inc. |
NexGen CompleteKnee Solution Stemmed Nonaugmentable Tibial component The NexGen®® system is a sem... | 2 | 11/26/2012 | Zimmer, Inc. |
-