Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K111663 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE, Item # 856204008. Devices are packaged... | 2 | 03/18/2022 |
FEI # 1825034 Biomet, Inc. |
| A.L.P.S. MIS Calcaneus Locking Plate LG RT F.A.S.T. Guide inserts, Item Number: 816209003,UDI: 00887... | 2 | 04/03/2018 |
FEI # 1825034 Zimmer Biomet, Inc. |
| A.L.P.S., 3.5mm x 60 mm Cortical Locking Screw. Bone fixation screw | 2 | 07/10/2015 |
FEI # 1825034 Biomet, Inc. |
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