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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 500 Results *
Recall Date to: 09/12/2015 Firm: Philips Medical Systems
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Allura Xper FD10 x-ray system 2 02/28/2006 Philips Medical Systems North America Co. Phillips
Allura Xper FD10/10 Biplane X-ray system. Intended for use in cardiovascular and vascular x-ray ima... 2 10/22/2010 Philips Medical Systems North America Co. Phillips
Allura Xper FD10/10 x-ray system 2 02/28/2006 Philips Medical Systems North America Co. Phillips
Allura Xper FD20 X-Ray System, Release 2.2, Philips Medical Systems, Bothell, WA 98021 2 12/07/2007 Philips Medical Systems North America Co. Phillips
Allura Xper FD20/10, Release 1.2, Philips Medical Systems, Bothell, WA 98021 2 12/07/2007 Philips Medical Systems North America Co. Phillips
Automated External Defibrillator (AED) of brand name "Philips HeartStart HS1 Home" (Model Number M5... 2 06/28/2010 Philips Medical Systems
Automated External Defibrillator (AED) of brand name "Philips HeartStart FRx" (Model number 861304).... 2 06/28/2010 Philips Medical Systems
Automated External Defibrillator(AED) of brand name "Philips HeartStart HS1 OnSite" (Model number M5... 2 06/28/2010 Philips Medical Systems
Axis Gamma Camera, Scintillation (gamma) camera, Philips Medical System, Cleveland, OH 44143 3 09/19/2008 Philips Medical Systems (Cleveland) Inc
BIPLANE X-ray Imaging Systems included Allura XPER FD10/10, FD20/10, FD20/20, Integris BH5000, and I... 2 09/22/2010 Philips Medical Systems North America Co. Phillips

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