Medical Device Recalls
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1 result found
Recall Number: Z-0506-2018 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Peripheral Diamondback 1.50 Solid OAD, a percutaneous orbital atherectomy system indicated for use a... | 2 | 10/11/2018 |
FEI # 3004742232 Cardiovascular Systems Inc |
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