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U.S. Department of Health and Human Services

Medical Device Recalls
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181 to 190 of 500 Results *
Recall Date to: 02/26/2015
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BodyGuard 323 pump, models 100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS, 100-603XSA and 100-60... 2 02/19/2015 CME America, LLC
Echostar Spica 1.5T MRI system, for magnetic resonance imaging of the body. 1 02/18/2015 Alltech Medical Systems America Inc
This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR4... 1 02/18/2015 GE Healthcare
Alive ECG App 2.1.2 ( a medical device application for the Apple iOS operating system, intended to b... 3 02/18/2015 Alivecor SFO
Mallory Head 4 Finned Acetabular Shell 50 mm, PN 13-104150, hip prosthesis component (Ringloc) 2 02/17/2015 Biomet, Inc.
Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component. 2 02/17/2015 Biomet, Inc.
Artis One; The Artis One is an angiography system developed for diagnostic interventional procedures... 2 02/17/2015 Siemens Medical Solutions USA, Inc
R®SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral... 2 02/17/2015 Teleflex, Inc.
Pulsiocath PiCCO ProAQT Monitoring Kit, single-use cardiac output (CO) sensor, one unit per plastic ... 2 02/17/2015 Pulsion Medical Inc
HARMONIC ACE Curved Shears Instructions for Use, 5MM, IS1200; for use with the da Vinci Standard Sur... 2 02/13/2015 Intuitive Surgical, Inc.

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