Medical Device Recalls
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1 result found
510(K) Number: K130608 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic sterile single-use blades that are components of the StraightShot M Series Handpiece and F... | 2 | 10/21/2021 | Medtronic Xomed, Inc. |
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