Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K033363 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
ZIMMER UNI HIGH FLEX PRECOAT FEM prosthesis, knee, femorotibial, non-constrained, cemented, metal/... | 2 | 02/22/2016 | Zimmer Biomet, Inc. |
ZUK PRC FEM SZB RMED/LLAT® ZUK PRC FEM SZC LMED/RLAT® ZUK PRC FEM SZC RMED/LLAT® NGU PRC FEM SZD ... | 2 | 03/14/2018 | Zimmer Biomet, Inc. |
Zimmer® Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disab... | 2 | 10/25/2013 | Zimmer, Inc. |
-