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U.S. Department of Health and Human Services

Medical Device Recalls

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Product Description
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Allura Xper FD10, FD10 C, and FD10 F; Model Numbers: 722026 722010 722003 722002 722001 Intended... 2 Jan-30-2016 Philips Electronics North America Corporation
Allura Xper FD10/10; Model Numbers: 722027 722011 722005 Intended for Cardiovascular and vascular... 2 Jan-30-2016 Philips Electronics North America Corporation
INTEGRIS V5000: Model Number: 72248 The Philips INTEGRIS 3000 I 5000 system is intended for inter... 2 Jan-30-2016 Philips Electronics North America Corporation
INTEGRIS BH5000; Model Number: 72247 The Philips INTEGRIS 3000 I 5000 system is intended for inte... 2 Jan-30-2016 Philips Electronics North America Corporation
INTEGRIS H5000; Model Number: 72246 The Philips INTEGRIS 3000 I 5000 system is intended for inter... 2 Jan-30-2016 Philips Electronics North America Corporation
INTEGRIS V3000; Model Number: 72243, 72244, 72245 The Philips INTEGRIS 3000 I 5000 system is inte... 2 Jan-30-2016 Philips Electronics North America Corporation
INTEGRIS BH3000; Model Number: 72242 The Philips INTEGRIS 3000 I 5000 system is intended for inte... 2 Jan-30-2016 Philips Electronics North America Corporation
INTEGRIS BN/BV3000; Model Number: 72240 The Philips INTEGRIS 3000 I 5000 system is intended for i... 2 Jan-30-2016 Philips Electronics North America Corporation
INTEGRIS HM3000; Model Number: 72239 The Philips INTEGRIS 3000 I 5000 system is intended for inte... 2 Jan-30-2016 Philips Electronics North America Corporation
INTEGRIS H3000; Model Number: 72238 The Philips INTEGRIS 3000 I 5000 system is intended for inter... 2 Jan-30-2016 Philips Electronics North America Corporation

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