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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 500 Results *
Recall Date to: 07/30/2015
 
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Spiral Gold Hollow Fiber Oxygenator with Duraflow Treatment, a hollow fiber membrane oxygenator. 2 12/02/2002 Jostra-Bentley Corporation
GEM DR Model 7271 Implantable Cardioverter-Defibrillator (ICD) 2 12/02/2002 Medtronic,Inc/Rice Creek Facil
Gambro ClinicalKit Safety Kit 16G, Catalog Number 0141080404C. Packaged 30 kits per case. Each kit c... 2 12/02/2002 Gambro Renal Products
Gambro ClinicalKit Safety Kit 15G, Catalog Number 0141080405C. Packaged 30 kits per case. Each kit c... 2 12/02/2002 Gambro Renal Products
Misys Laboratory versions 5.23 and 5.3 with Callback 2 12/05/2002 Sunquest Information Systems
Product is packaged and labeled as: ''Cordis PRECISE Nitinol Stent Transhepatic Billiary System'', C... 2 12/05/2002 Cordis Corporation
Computed Tomography system, Diagnostic Imaging: Somatom Sensation 4 Somatom Volume Zoom Somatom... 2 12/05/2002 Siemens Medical Systems Inc
Drop Hooks for Xact (tm) Lo-Pro with Removeable Drop Seat, Xact Integrated, and Xact Individual with... 2 12/05/2002 Action Products Incorporated
Misys Laboratory version 5.2 with Results Interface 14 2 12/05/2002 Sunquest Information Systems
Misys Laboratory versions 5.2, 5.23, or 5.3 with ADT Interface to CoPathPlus. 2 12/11/2002 Sunquest Information Systems

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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