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U.S. Department of Health and Human Services

Medical Device Recalls
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261 to 270 of 500 Results *
Recall Date to: 05/07/2015
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Product is labeled as ''Oto-''Flex Bur'', Medtronic-Xomed brand, packed into a sterile pouch. Produc... 2 03/20/2003 Medtronic Xomed, Inc.
LTX Endosseous Implant 6.0 mm X 11.5 mm and also LTX Endosseous Implant 5.0 mm X 15 mm, Sterile, 3 03/20/2003 Implant Innovations, Inc.
TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016. 2 03/20/2003 Interpore Cross International Inc
Sarns MP4 Cardioplegia Sets; catalog number 15501. 2 03/20/2003 Terumo Cardiovascular Systems Corp
Medi-Tech Magic Torque Glidex hydrophilic coated guidewire, .035 inch/180 cm and .035 inch/260 cm le... 3 03/20/2003 Symbiosis Corp.
CryoValve Allograft, Heart valve 2 03/21/2003 Cryolife Inc
X-ray, Computed Tomography, Model TSX101A 3 03/21/2003 Toshiba American Med Sys Inc
ECAT Software Versions V7.1.1b, V7.2, V7.2.1, and V7.2.2 used in the following PET (Positron Emissio... 2 03/21/2003 Cti Pet Systems Inc
CryoValve Allograft heart valve 2 03/21/2003 Cryolife Inc
COBAS INTEGRA Creatinine Jaffe for use on the INTEGRA 400, 700 and 800 analyzers; system ID # 076434... 2 03/21/2003 Roche Diagnostics Corp.

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