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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-2841-2020 - Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 34cc IAB (Japan) Kit P/N: 0684-00-0545-01- Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Com...
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2
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08/21/2020
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FEI # 1000222374 Datascope Corporation
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Z-2842-2020 - Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 40cc IAB (Japan) - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Fail...
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2
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08/21/2020
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FEI # 1000222374 Datascope Corporation
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Z-2843-2020 - Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 35cc IAB (Japan) Kit P/N: 0684-00-0607 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surger...
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2
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08/21/2020
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FEI # 1000222374 Datascope Corporation
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Z-2844-2020 - Datascope Intra-Aortic Ballon Catheters (IABs)-TRANS-RAY PLUS 7.5Fr 40cc IAB (Japan) Kit P/N: 0684-00-0608 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surger...
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2
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08/21/2020
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FEI # 1000222374 Datascope Corporation
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Z-2845-2020 - Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 30cc IAB (Japan) Kit P/N: 0684-00-0559-01 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surg...
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2
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08/21/2020
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FEI # 1000222374 Datascope Corporation
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Z-2846-2020 - Datascope Intra-Aortic Ballon Catheters (IABs)-YAMATO PLUS-R 7.5Fr 35cc IAB (Japan) Kit P/N: 0684-00-0560-01 - Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surg...
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2
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08/21/2020
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FEI # 1000222374 Datascope Corporation
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Z-2832-2020 - Datascope Intra-Aortic Balloon Catheters (IABs)-MEGA 7.5Fr 40cc IAB Kit P/N: 0684-00-0295-01, 0684-00-0295-01U, 0684-00-0295-02, 0684-00-0295-02U, 0684-00-0295-05, 0684-00-0295-07, 0684-00-0295-09, 06...
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2
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08/21/2020
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FEI # 1000222374 Datascope Corporation
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