Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K990772 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Heartport Direct Flow Arterial Cannula, product code DFK24. The device is sold separately and also ... | 2 | 06/09/2006 | Ethicon, Inc. |
EndoReturn arterial cannula. The EndoReturn arterial cannula is indicated for patients undergoing c... | 3 | 01/09/2004 | Heartport Inc |
SoftClamp II arterial cannula is intended to deliver oxygenated blood for cardiopulmonary bypass dur... | 3 | 01/09/2004 | Heartport Inc |
Introducer Sheath is indicated for patients requiring introduction of catheters. Introducer Sheath ... | 3 | 01/09/2004 | Heartport Inc |
EndoReturn arterial cannula. The EndoReturn arterial cannula is indicated for patients undergoing c... | 3 | 01/09/2004 | Heartport Inc |
DirectFlow arterial cannula is intended to deliver oxygenated blood for cardiopulmonary bypass durin... | 3 | 01/09/2004 | Heartport Inc |
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