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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: 07/26/2014
 
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zimmer Anatomical Shoulder Glenoid S, cemented, sterile; REF 01.04214.340 PE Keeled Glenoid S, cem... 2 11/06/2012 Zimmer, Inc.
xTAG CYP2D6 Kit v3 IVD For use with Luminex 100/200 Instrument Luminex Molecular Diagnostics, Inc. 4... 2 08/31/2011 Luminex Corporation
ultraView Universal DAB Detection Kit, Part number: 760-500 (05269806001) This detection kit is i... 2 07/01/2011 Ventana Medical Systems Inc
uTASWako DCP, Lot TG340 2013.11, REF 995-60701, Wako Pure Chemical Industries, Ltd. 1-2 Doshomachi 3... 2 07/30/2013 Wako Life Sciences, Inc.
syngo.plaza, Model number 10592457. Intended use: radiological image processing system. 2 08/27/2012 Siemens Medical Solutions USA, Inc
syngo.plaza Image processing system 2 01/11/2012 Siemens Medical Solutions USA, Inc
syngo(R) Lab Data Manager and syngo(R) Lab Process Manager, all versions. This device is classifi... 2 08/31/2012 Siemens Healthcare Diagnostics, Inc.
syngo(R) Lab Data Manager - Version VA11B and VA12A Systems Securely consolidates data from multi... 2 12/03/2013 Siemens Healthcare Diagnostics, Inc.
syngo US Workplace Picture Archiving and Communication System, software version 2.0, Siemens Medica... 2 05/20/2008 Siemens Medical Solutions USA, Inc.
syngo RT Therapist and syngo RT Therapist Connect/MOSAIQ OIS. This correction applies to customers ... 2 01/11/2012 Siemens Medical Solutions USA, Inc

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