Medical Device Recalls
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1 result found
510(K) Number: K153233 |
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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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Orthofix Power Drill Torque Limiter, Sterile, Rx Only, Single Use; Sold individually and in the Gala... | 2 | 12/27/2017 | Orthofix Srl |
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