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U.S. Department of Health and Human Services

Medical Device Recalls
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111 to 120 of 500 Results *
Recall Date to: 12/22/2014
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Ceramic Femoral Head. Intended for use in total hip arthroplasty applications to replace the ar... 2 12/17/2014 DePuy Orthopaedics, Inc.
VERO Linear Accelerator System, Model Number MHI-TM2000, MHI Identifier M101-14021, Software Version... 2 12/17/2014 MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK
WECK Hemoclip® Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for u... 2 12/17/2014 Teleflex Medical
Bone Screw, self-tapping The Trilogy shells are available in three configurations; uni, multi, and ... 2 12/17/2014 Zimmer Manufacturing B.V.
Trinity biotech Captia (TM) Syphilis IgM Capture Test Kit, Product No./REF 800-935, Test Kit for 96 ... 3 12/16/2014 Clark Laboratories, Inc. (dba,Trinity Biotech USA)
Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebros... 3 12/16/2014 Aesculap, Inc.
Intended for both adult and pediatric patients for taking diagnostic radiographic exposures of the s... 2 12/16/2014 Philips Medical Systems, Inc.
Ascension Orthopedics PyroSphere CMC & PyroSphere TMT, intended to replace the joint between the fir... 2 12/16/2014 Integra LifeSciences Corp.
Q-Station Quantification Software. Q-Station 3.0 with a2DQ and/or aCMQ Q-Apps are affected. Model: ... 2 12/16/2014 Philips Ultrasound, Inc.
EPIQ 7 Ultrasound System, EPIQ 7 systems with software versions 1.0.x or 1.1.x with QLAB a2DQ and/or... 2 12/16/2014 Philips Ultrasound, Inc.

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