Medical Device Recalls
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1 result found
Recall Number: Z-1832-2017 |
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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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| HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product Usage: Is intended... | 1 | 04/25/2017 |
FEI # 3007042319 Heartware |
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