Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151881 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Orthex Large Bone Shoulder Bolt, model no. AS-17 | 2 | 11/22/2022 | OrthoPediatrics Corp |
Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN | 2 | 09/06/2022 | OrthoPediatrics Corp |
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