Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081475 |
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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 |
FEI # 1045254 Medtronic Xomed, Inc. |
| Saw Sagittal Catalog Number: ES 300; Saw Sagittal Refurbished Catalog Number: ES300-R; Saw Saggital,... | 2 | 06/28/2016 |
FEI # 1625507 Medtronic Sofamor Danek Usa, Inc - Dallas Distribution |
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