Medical Device Recalls
-
91 to 100 of 250 Results
510(K) Number: K100238 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 260MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 320MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 340MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 360MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 400MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 420MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 440MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 9MM X 460MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 260MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 130 DEG 11MM X 280MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
-