Medical Device Recalls
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31 to 40 of 250 Results
510(K) Number: K100238 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Affixus Hip Fracture Nail, LH 130 DEG 9MM X 440MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 11MM X 300MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 11MM X 380MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 11MM X 440MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 11MM X 460MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 13MM X 260MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 125 DEG 13MM X 320MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
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. |
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