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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1879-2024
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Arrow UltraFlex Intra-Aortic Balloon Catheter Kit, a) REF IAB-06830-U; b) REF IAB-06840-U; c) REF... 1 06/03/2024 FEI # 3013162291
ARROW INTERNATIONAL Inc.
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