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U.S. Department of Health and Human Services

Medical Device Recalls
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71 to 80 of 500 Results *
Recall Date to: 09/12/2015 Firm: Philips Medical Systems
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Product Description
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FDA Recall
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OmniDiagnost System 2 07/20/2004 Philips Medical Systems Sales & Service Region No. America
Philips Digital Diagnost VT 2 12/24/2003 Philips Medical Systems Sales & Service Region No. America
Digital Diagnost VE 2 12/24/2003 Philips Medical Systems Sales & Service Region No. America
Bucky Diagnost FS Part number 9890-010-83651 2 12/24/2003 Philips Medical Systems Sales & Service Region No. America
Diagnost 96 2 09/11/2003 Philips Medical Systems Sales & Service Region No. America
Diagnost 97 2 09/11/2003 Philips Medical Systems Sales & Service Region No. America
Diagnost 94 2 09/11/2003 Philips Medical Systems Sales & Service Region No. America
Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound imaging and fluid flow a... 2 03/20/2014 Philips Medical Systems North America Inc.
Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound imaging and fluid flow a... 2 03/20/2014 Philips Medical Systems North America Inc.
Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs). Product Usage... 2 03/19/2014 Philips Medical Systems North America Inc.

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