136 results
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18ms
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Sources: EU EUDAMED, US FDA
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Catalog A800061, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZC·August 5, 2021
Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327; The TwinTube sample line 240cm is used in the Vyntus CPX. The TwinTube sample line 240cm is connected to the adapter for DVT. Twin Tube Probenschlauch (707004), which is sold outside the US only. Used in breath analysis for metabolic response study.
FDA Recall
Open, Classified
·Vyaire Medical, Inc. Leibnizstr. 7 Hochberg Germany·Product code BZC·April 8, 2024
Bard Foley procedural trays packaged in breather bags. The product is packaged ten units in each shipper box, and are sold sterile for single use. Used to catheterize patients. The finished trays are sold in Tyvek breather bags.
FDA Recall
Terminated
·C.R. Bard, Inc., Urological Division·Product code EZC·June 29, 2012
TMA Archwires, Part Number 211-1402, Lot Number 10K291, Product Description and Intended Use: The intended use of this device is an archwire during orthodontic treatment.
FDA Recall
Terminated
·Ormco Corporation·Product code DZC·March 15, 2011
Resp Profile Monitor, 8100 Cosmo+, Respironics/Philips product. Used to provide spirometric, carbon dioxide and pulse oximetry monitoring.
FDA Recall
Terminated
·Philips Healthcare Inc.·Product code BZC·November 19, 2009
Catalog A902616, SureStep" Foley Tray, Bardex" I.C., Lubricath", Urine Meter
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZC·August 5, 2021
Catalog A800360, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
FDA Recall
Open, Classified
·C.R. Bard Inc·Product code EZC·August 5, 2021
GE OEC 9900 Elite ESP fluoroscopic x-ray system. GE Healthcare, Surgery, Salt Lake City, UT. The system is intended to provide an x-ray display of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 29, 2008
OEC 9800 Image Intensified fluoroscopic x-ray system (includes OEC 9800, OEC FluoroTrak 9800 Plus, OEC 9800 Plus, and OEC 9800MD Motorized C-arm System), GE Healthcare, Surgery, Salt Lake City, UT.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·April 15, 2008
GE OEC 9800 Fluoroscopic X-Ray System, GE Healthcare, Surgery, Salt Lake City, Utah. The intended use of this device is to perform mobile fluoroscopic examination of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 12, 2008
GE OEC 9600 C-arm Fluoroscopy System, GE Healthcare, Surgery, Salt Lake City, Utah.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·July 2, 2008
OEC 9900 Elite Image-intensified fluoroscopic x-ray system (includes OEC 9900 Elite Fluoroscopy System and 9900 EliteMD Motorized C-arm System), GE Healthcare, Surgery, Salt Lake City, UT.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·April 15, 2008
GE OEC 9900 Elite Fluoroscopic X-Ray System, GE Healthcare, Surgery, Salt Lake City, Utah. The intended use of this device is to perform mobile fluoroscopic examination of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 12, 2008
InstaTrak 3500 Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code LLZ·December 13, 2004
GE Healthcare OEC 9900 mobile fluoroscopic x-ray system
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·December 14, 2007
FluroTrak 9800 Plus Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·December 13, 2004
ENTrak Plus Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code LLZ·December 13, 2004
InstaTrak 3000 Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code LLZ·December 13, 2004
ENTrak Navigation and Visualization System
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code LLZ·December 13, 2004
GE OEC 9900 Elite GSP fluoroscopic x-ray system GE Healthcare, Surgery, Salt Lake City, UT. The system is intended to provide an x-ray display of human anatomy.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·August 29, 2008