Medical Device Recalls
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1 result found
Recall Number: Z-1061-2016 |
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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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| RediGuard IAB: 7Fr 30cc; Product Code: IAB-S730C The Arrow¿ IAB is utilized for intra aortic ball... | 1 | 03/11/2016 |
FEI # 3010532612 Arrow International, Inc., Division of Teleflex Medical Inc. |
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