45 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Terminated
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iba COMPASS SW Version 3.0, Catalog Number CS10-100 (medical linear accelerator) radiological
FDA Enforcement
Class II
·Terminated·Iba Dosimetry Gmbh·December 18, 2013
Maquet Getinge- BEQ-TOP 54500 BSW-McLANE 3/8 Quadrox iD Material:709000496R01
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019
Maquet Getinge- BEQ-TOP 54500 BSW-McLANE 3/8 Quadrox iD Material:709000496R01
FDA Enforcement
Class II
·Terminated·Maquet Cardiovascular, LLC·June 5, 2019
Carestream DRX Evolution System, X-Ray System --- The DRX-Evolution system is a permanently installed diagnostic x-ray system for generation of x-rays for examination of various anatomical regions.
FDA Recall
Terminated
·Carestream Health Inc.·Product code KPR·June 3, 2013
RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use
FDA Recall
Terminated
·Ability Dynamics LLC·Product code ISW·June 2, 2014
Polyflex Esophageal Stent 20/16mm x 90mm
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·April 16, 2003
Polyflex Esophageal Stent 20/16mm x 120mm
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·April 16, 2003
Boston Scientific Ultraflex Covered large Esophageal Stent System - Distal Release (23/28/10/7) Material/UPN/Catalog Number: M00514200
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·July 15, 2010
Ultraflex Esophageal Stent System. Uncovered - Distal Release - 18/23/15. Catalog Number M00513720. Single Use, Rx only. Boston Scientific, Natick, MA 01760. Intended for maintaining esophageal luminal patency in esophageal structures caused by intrinsic and/or extrinsic malignant tumors only and occlusion of concurrent esophageal fistulas.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·May 17, 2010
Ultraflex Esophageal Stent System. Uncovered - Proximal Release - 18/23/10. Catalog Number M00513810. Single Use, Rx only. Boston Scientific, Natick, MA 01760. Intended for maintaining esophageal luminal patency in esophageal structures caused by intrinsic and/or extrinsic malignant tumors only and occlusion of concurrent esophageal fistulas.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·May 17, 2010
Polyflex Esophageal Stent 25/21mm x 150mm
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·April 16, 2003
BiOM Rechargeable Li Ion 22.2 V Battery and BiOM Lithium Battery Charger sold as an accessory to the BiOM lower leg system: Product Number: 2001249 BiOM Battery Product Number: 2001240 BiOM Charger
FDA Recall
Terminated
·iwalk inc·Product code ISW·October 26, 2012
Polyflex Esophageal Stent 25/21mm x 90mm
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·April 16, 2003
Polyflex Esophageal Stent 23/18mm x 90mm
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·April 16, 2003
Ultraflex Esophageal Stent System. Uncovered - Proximal Release - 18/23/15. Catalog Number M00513830. Single Use, Rx only. Boston Scientific, Natick, MA 01760. Intended for maintaining esophageal luminal patency in esophageal structures caused by intrinsic and/or extrinsic malignant tumors only and occlusion of concurrent esophageal fistulas.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·May 17, 2010
Ultraflex Esophageal Stent System. Covered - Large - Distal Release - 23/28/10/7. Catalog Number M00514200. Single Use, Rx only. Boston Scientific, Natick, MA 01760. Intended for maintaining esophageal luminal patency in esophageal structures caused by intrinsic and/or extrinsic malignant tumors only and occlusion of concurrent esophageal fistulas.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·May 17, 2010
Ultraflex Esophageal Stent System. Covered - Proximal Release - 18/23/15/12. Catalog Number M00513860. Single Use, Rx only. Boston Scientific, Natick, MA 01760. Intended for maintaining esophageal luminal patency in esophageal structures caused by intrinsic and/or extrinsic malignant tumors only and occlusion of concurrent esophageal fistulas.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·May 17, 2010
Ultraflex Esophageal Stent System. Covered - Large - Proximal Release - 23/28/12/9. Catalog Number M00514250. Single Use, Rx only. Boston Scientific, Natick, MA 01760. Intended for maintaining esophageal luminal patency in esophageal structures caused by intrinsic and/or extrinsic malignant tumors only and occlusion of concurrent esophageal fistulas.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·May 17, 2010
Boston Scientific Ultraflex Covered Esophageal Stent System - Proximal Release (18/23/12/9) Material/UPN/Catalog Number: M00513850
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·July 15, 2010
Ultraflex Esophageal Stent System. Covered - Proximal Release - 18/23/10/7. Catalog Number M00513840. Single Use, Rx only. Boston Scientific, Natick, MA 01760. Intended for maintaining esophageal luminal patency in esophageal structures caused by intrinsic and/or extrinsic malignant tumors only and occlusion of concurrent esophageal fistulas.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code ESW·May 17, 2010