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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0336-2022 - Cardiosave Hybrid IntraAortic Balloon Pump. Model UDI 0998-00-0800-31 10607567109053 0998-00-0800-32 10607567111117 0998-00-0800-33 10607567109008 0998-00-0800-34 10607567111940 09... 1 12/30/2021 Datascope Corp.
Z-0337-2022 - Cardiosave Rescue IntraAortic Balloon Pump. Model UDI 0998-00-0800-75 10607567112312 0998-00-0800-83 10607567108407 0998-00-0800-85 10607567113449 1 12/30/2021 Datascope Corp.
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