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  • Device 2359
  • Manufacturer 570
  • Event 124969
  • Implant 153
Name Classification Manufacturer Risk Class Country Source
LifeStream Balloon expandable vascular Covered Stent ClearStream Technologies Ltd. Germany BAM
Use for the Recovery® G2 Filter BARD Germany BAM
Bard® LUMINEXX® Endoscopic Biliary Stent and Bard® memotherm® Colorectal Stent Angiomed Germany BAM
Bard® LUMINEXX® 3 Biliary and Vascular Stents and Bard® LUMINEXX® 6 F Vascular Stents Angiomed Germany BAM
the BD Preset 3ml. Arterial Gas Syringe, Becton Dickinson and Company Germany BAM
the Bard Lifestent Vascular Stent System Angiomed Germany BAM
several lots of the LifeStent Solo Vascular Stent System. The recall is only for products of the old design Angiomed GmbH & Co. Medizintechnik KG Germany BAM
Vivexx Carotid Stent Angiomed GmbH & Co. Medizintechnik KG Germany BAM
“M.R.I. Implanted Port“ port system BARD Germany BAM
product Low Profile Port with 6.6 Fr Single Lumen Broviac Catheter Bard Access Systems Division Germany BAM
multi-length ureteral stents Bard Limited Germany BAM
Ventralight™ ST Mesh with Echo PS™ Positioning System and Composix™ L/P Mesh with Echo PS™ Positioning System Bard® Germany BAM
IntrepideTM coronary stent system ClearStream Germany BAM
Multi-length ureteral stents Bard Medical Division Sweden SMPA
Bard Ventralight ST mesh with Echo PS Positioning System and Bard Composix L / P Mesh with Echo PS Positioning System Davol Inc. Sweden SMPA
DuaLok Breast Localisation Wire Bard Peripheral Vascular Sweden SMPA
Life stent vascular stent system Angiomed GmbH & Co. Medizintechnik KG Sweden SMPA
MRI Implanted port Bard Access Systems Sweden SMPA
Device Recall PowerPICC SOLO Catheter General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall PowerPICC SOLO Catheter General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall PowerPICC SOLO Catheter General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall Bard Distaflo Vascular Bypass Graft Cardiovascular Devices Bard Peripheral Vascular Inc 2 United States USFDA
Device Recall Bard Denali IVC Filter Cardiovascular Devices Bard Peripheral Vascular Inc 2 United States USFDA
Device Recall Bard Access Marketing Brochures General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
Device Recall PowerPICC SOLO Catheter General Hospital and Personal Use Devices Bard Access Systems 2 United States USFDA
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About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.