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U.S. Department of Health and Human Services

Medical Device Recalls
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211 to 220 of 500 Results *
Recall Date to: 07/14/2014
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cobas 8000 analyzer series Operators Manual Roche cobas Filter label: Filter (N) Mat. No 0314977... 2 06/14/2014 Roche Diagnostics Operations, Inc.
cobas 6000 analyzer series Operators Manual Roche cobas; Filter label: Filter (N) Mat. No 0314977... 2 06/14/2014 Roche Diagnostics Operations, Inc.
cobas 4800 BRAF V600 Mutation Test for In Vitro Diagnostic Use Roche Molecular Systems, Inc., Pr... 3 11/02/2012 Roche Molecular Systems, Inc.
chromID Salmonella Agar, Reference No. 43621. A selective isolation and differentiation medium fo... 2 10/28/2013 bioMerieux, Inc.
cardioPAT Cardiovascular Perioperative Autotransfusion System, Model: LN 2050-110-E and Disposables... 2 11/23/2005 Haemonetics Corporation
c.cam Gamma Camera, Model No: 9VIR1200; Tomography System (Emission Computed); Siemens Medical Solut... 2 12/19/2007 Siemens Medical Solutions USA, Inc.
c.cam Gamma Camera, Model 9VIR1200; Siemens Medical Solutions USA, Inc., Molecular Imaging, 2501 N. ... 2 06/06/2007 Siemens Medical Solutions USA, Inc.
bluephase style Light probe Pin-point 6>2 mm black REF # 636 241. The accessory is a pin point ligh... 2 06/09/2014 Ivoclar Vivadent, Inc.
biphasic LIFEPAK 500 automated external defibrillators (AEDs) with software version 4.4 or lower; Pa... 2 08/04/2007 Medtronic Emergency Response Systems, Inc.
bioMerieux, BacT/ALERT® FA Culture Bottles, bioMerieux, Inc., Durham, NC 27704 2 01/04/2008 bioMerieux, Inc.

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