Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K190085 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM | 2 | 04/14/2023 | Smith & Nephew, Inc. |
JOURNEY II UNI RESECTION PREP TRIAL, LEFT MEDIAL/ RIGHT LATERAL - Product Usage: The JOURNEY II Uni ... | 2 | 05/27/2020 | Smith & Nephew, Inc. |
JOURNEY II UNI RESECTION PREP TRIAL, RIGHT MEDIAL/ LEFT LATERAL - Product Usage: The JOURNEY II Uni ... | 2 | 05/27/2020 | Smith & Nephew, Inc. |
-