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