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U.S. Department of Health and Human Services

Medical Device Recalls
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221 to 230 of 500 Results *
Recall Date to: 04/08/2014
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Product Description
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i-STAT G3+ Cartridge pH, pCO2 and pO2 measurements are used in the diagnosis, monitoring and trea... 2 03/27/2014 Abbott Point Of Care Inc.
Morph AccessPro Steerable Introducer; 6F Introducer, 90 cm working length: Single use only. Bio... 2 03/27/2014 Biocardia, Inc.
FIBERNET Embolic Protection System: Recommended Vessel Diameter 5.0 -6.0 mm, Maximum Guidewire Diam... 2 03/27/2014 Medtronic Vascular, Inc.
FIBERNET Embolic Protection System: Recommended Vessel Diameter 3.5 0 5.0 mm, Maximum Guidewire Dia... 2 03/27/2014 Medtronic Vascular, Inc.
Morph AccessPro Steerable Introducer; 6F Introducer, 45 cm working length Single use only. BioCar... 2 03/27/2014 Biocardia, Inc.
FIBERNET Embolic Protection System: Recommended Vessel Diameter 6.0 -7.0 mm, Maximum Guidewire Diam... 2 03/27/2014 Medtronic Vascular, Inc.
Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray 2 03/27/2014 Siemens Medical Solutions USA, Inc
PowerPort Slim Implantable Port, indicated for patient therapies requiring repeated access to the va... 2 03/27/2014 Bard Access Systems
D-10" Hemoglobin Testing System, Model number: 220-0220 Manufactured by: Bio-Rad Laboratories,... 2 03/27/2014 Bio-Rad Laboratories, Inc.
Ovation Prime Abdominal Stent Graft System; Manufacturer: TriVascular, Inc. 3910 Brickway Blvd. Sa... 2 03/26/2014 Trivascular, Inc

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