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  • Device 1
  • Manufacturer 1
  • Event 124969
  • Implant 0
Name Date Date initiated Country Source
Recall of Device Recall Arrow Pressure Injectable PICC Kit 2017-03-20 United States USFDA
Recall of Device Recall ETEST Ceftriaxone 2017-01-01 United States USFDA
Recall of Device Recall NMT Patient Cable (989803174581) 2017-05-04 United States USFDA
Recall of Device Recall Willscher Vas Reapproximator Set 2017-05-01 United States USFDA
Recall of Device Recall LATARJET EXPERIENCE Coracoid Top Hat Drill 2017-05-12 United States USFDA
Recall of Device Recall Willscher Vas Skewers 2017-05-01 United States USFDA
Recall of Device Recall Willscher Vas Reapproximator Plate 2017-05-01 United States USFDA
Recall of Device Recall Endoscopic Curved Needle 2017-05-01 United States USFDA
Recall of Device Recall LapSac Introducer 2017-05-01 United States USFDA
Recall of Device Recall LapSac Introducer Set 2017-05-01 United States USFDA
Recall of Device Recall Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD 2017-05-02 United States USFDA
Recall of Device Recall Proteus Plus and Proteus ONE 2017-02-09 United States USFDA
Recall of Device Recall SmartMonitor 2 PS/PSL 2017-05-01 United States USFDA
Recall of Device Recall Mobius 3D 2015-02-23 United States USFDA
Recall of Device Recall Electrophysiology catheter cables 2017-05-08 United States USFDA
Recall of Device Recall Toshiba Angio WorkStation (XIDFAWS801) 2017-02-01 United States USFDA
Recall of Device Recall Nexstim 2017-03-14 United States USFDA
Recall of Device Recall Nexstim 2017-03-14 United States USFDA
Recall of Device Recall Conformer Medium with holes (sterile) 2002-11-29 United States USFDA
Recall of Device Recall Artis zee angiographic xray system 2017-02-03 United States USFDA
Recall of Device Recall Opteryx Variable Rescue Screw 2017-05-05 United States USFDA
Recall of Device Recall Adenovirus (20/11 & 2/6) 2017-05-05 United States USFDA
Recall of Device Recall LeadCare Blood Lead Testing System 2017-05-23 United States USFDA
Recall of Device Recall LeadCare II Blood Lead Testing System 2017-05-23 United States USFDA
Recall of Device Recall Estrogen Receptor (EP1) 2017-05-05 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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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.