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U.S. Department of Health and Human Services

Medical Device Recalls
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151 to 160 of 500 Results *
Recall Date to: 10/25/2014
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Product Description
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FDA Recall
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ArcPoint Labs 10 Panel Dip Screen (BAR), Part No. APD-10M. The ArcPoint Labs Dip Drug Screen Dip ... 2 10/16/2014 Ameditech Inc
VITROS 4600 Chemistry System (VITROS 5,1 FS System family member), System Product Code 6802445. T... 2 10/16/2014 Ortho-Clinical Diagnostics
VITROS 5600 Integrated System, System Product Code 6802413. For use in the in vitro quantitative,... 2 10/16/2014 Ortho-Clinical Diagnostics
Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety of elbow joint repla... 2 10/16/2014 Biomet, Inc.
Multi-Lumen Central Venous Catheterization Kit 2 10/16/2014 Arrow International Inc
EndoWrist Stapler 45 instrument for the da Vinci Si System Model Number: IS3000 Product U... 2 10/16/2014 Intuitive Surgical, Inc.
AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities. 2 10/15/2014 Primus Medical LLC
Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pre-connected Part Numbe... 1 10/15/2014 Covidien LLC
Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number: 20660 1 10/15/2014 Covidien LLC
Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotranspa... 1 10/15/2014 Covidien LLC

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