Medical Device Recalls
-
1 to 6 of 6 Results
510(K) Number: K070978 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Segmental fluted stem, 18x250mm bwd, Sterile, | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
Segmental fluted stem, 19x250mm bwd, Sterile, Rod, fixation, intramedullary and accessories- Speci... | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
Segmental malefemale taper, 200mm, Sterile, Rod, fixation, intramedullary and accessories- Specifi... | 2 | 03/20/2017 | Zimmer Biomet, Inc. |
Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201)... | 2 | 02/26/2018 | Zimmer Biomet, Inc. |
Zimmer Segmental Systems; Polyethylene Inserts, Size B. Designed to address significant bone loss... | 2 | 01/17/2014 | Zimmer, Inc. |
Zimmer Segmental Systems; Polyethylene Inserts, Size C. Knee replacement. | 2 | 01/17/2014 | Zimmer, Inc. |
-