Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-2033-2017 - Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature. | 2 | 05/04/2017 |
FEI # 1118880 Terumo Medical Corporation |
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