Medical Device Recalls
-
1 to 2 of 2 Results
Related Medical Device Recalls |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Z-0628-2018 - AGC 2000 LP Patella, labeled as AGC Porous Patellar Med, Model Number 150804. Product Usage: For use in Total Knee Arthroplasty. | 2 | 02/15/2018 | Zimmer Biomet, Inc. |
Z-0627-2018 - AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For use in Total Knee Arthroplasty. | 2 | 02/15/2018 | Zimmer Biomet, Inc. |
-