Medical Device Recalls
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1 to 10 of 250 Results
510(K) Number: K100238 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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AFFIXUS Lag Screw Drill, REF 2112-01-303, Non-Sterile, DePuy Orthopaedics, Inc., Warsaw, IN; DePuy... | 2 | 03/22/2011 | Depuy Orthopaedics, Inc. |
AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail System is intended to treat stabl... | 2 | 06/01/2017 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 440MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, 125 DEG 11MM X 180MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, 125 DEG 9MM X 180MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, 130 DEG 11MM X 180MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, 130 DEG 9MM X 180MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 320MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 360MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
Affixus Hip Fracture Nail, LH 125 DEG 11MM X 440MM | 2 | 01/29/2018 | Zimmer Biomet, Inc. |
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