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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 276 Results
Product: arn Recall Date to: 10/09/2014
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Model Kodak 2100 Intraoral X-Ray System, Catalog Numbers 5303144, 8011579 -- Carestream Health, Inc.... 2 03/04/2014 Carestream Health Inc.
New Label: EtchMaster ***Cordless Handpiece***P/N 797 www.GromanDental.com 1800-906-9298 HAZARD WARN... 3 01/13/2012 Groman Inc.
Brand Name: QuietCare, Model Numbers QC200403, v.02; QC200403, v.03; QC200403, v.04 -- Classificatio... 3 06/05/2012 Intel-GE Care Innovations LLC
User Manual addendum, TORS for da Vinci Surgical System IS 1200, IS 2000 and IS 3000. Product Us... 2 05/29/2013 Intuitive Surgical, Inc.
Shoulder Flex Massage Device Device is an electric personal massage device labeled in part: "Sho... 1 11/10/2011 King International
ConMed Linvatec Hall Surgical Blades, Sterile ST REPL BLADE/SARNS STERNUM SAW, Catalog # 0050592330... 2 01/15/2009 Linvatec Corp.
REF 87100 87k Arthroscopy Tubing Set. For use with the 87k Arthroscopy Pump (87000). STERILE EO. R... 2 08/09/2010 Linvatec Corp. dba ConMed Linvatec
Vitatron C-Series C60DR DDDR Dual Chamber Rate Responsive Pacemaker includes the following models: C... 2 07/07/2007 Medtronic Inc. Cardiac Rhythm Managment
Vitatron T-Series Dual Chamber pacemaker T60 DR, model T60A1. The Vitatron C60 DR is a dual chamber ... 2 07/07/2007 Medtronic Inc. Cardiac Rhythm Managment
An external nasal splint is a rigid or partially rigid device intended for the use externally for im... 2 03/17/2011 Medtronic Xomed, Inc.
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