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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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Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 099...
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2
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10/07/2021
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Datascope Corp.
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Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 099...
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2
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09/30/2021
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Datascope Corp.
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CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX
Li-Ion ...
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2
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03/02/2017
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Maquet Datascope Corp - Cardiac Assist Division
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Cardiosave Hybrid and rescue IABP
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2
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03/25/2016
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Maquet Datascope Corp - Cardiac Assist Division
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Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP)
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2
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02/23/2015
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Maquet Datascope Corp - Cardiac Assist Division
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CARDIOSAVE Intra-Aortic Balloon Pump and CS300 Intra-Aortic Balloon Pump; and, non-sterile, not for ...
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2
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02/07/2015
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Maquet Datascope Corp - Cardiac Assist Division
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CARDIOSAVE Intra-Aortic Balloon Pump
An electromechanical system used to inflate and deflate intr...
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2
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01/09/2013
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Maquet Cardiovascular, LLC
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Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-...
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1
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03/09/2023
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Datascope Corp.
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Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Containing Coiled Cord cable (part number 0012-...
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1
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03/09/2023
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Datascope Corp.
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Cardiosave Rescue IntraAortic Balloon Pump.
Model UDI
0998-00-0800-75 1060756711...
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1
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12/30/2021
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Datascope Corp.
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