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  • Device 3
  • Manufacturer 3
  • Event 124969
  • Implant 0
Name Date Date initiated Country Source
Recall of Device Recall Central Venous Catheter Set Triple Lumen Polyurethane 2017-07-31 United States USFDA
Recall of Device Recall Central Venous Catheter Tray Triple Lumen Polyurethane 2017-07-31 United States USFDA
Recall of Device Recall Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane 2017-07-31 United States USFDA
Recall of Device Recall Central Venous Tray Triple Lumen Polyurethane Catheter 2017-07-31 United States USFDA
Recall of NEXGEN LPS-FLEX PRECOAT FEMORAL SIZE E-LT || This device is indicated for patients with severe knee pain and disability 2017-11-29 United States USFDA
Recall of Device Recall Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic Impregnated 2017-07-31 United States USFDA
Recall of Device Recall FUTURO (TM) SPORT, QUICK STRAP ANKLE SUPPORT 2018-01-31 United States USFDA
Recall of Device Recall ACE (TM) BRAND, DELUXE ANKLE BRACE 2018-01-31 United States USFDA
Recall of Device Recall GEOMED CABG PACK PGYBK A & B 2018-01-22 United States USFDA
Recall of Device Recall NEXGEN LPSFLEX MOBILE AND LPSMOBILE BEARING KNEE SYSTEM 2017-11-29 United States USFDA
Recall of Device Recall Syngo.plaza Picture Archiving and Communication System 2017-08-18 United States USFDA
Recall of Device Recall Innova Vascular SelfExpanding Stent System 180mm 2017-11-06 United States USFDA
Recall of Device Recall Medtronic AFFINITY NT, Cardiotomy/Venous Reservoir (CVR) with Filter, 540 2018-01-16 United States USFDA
Recall of Device Recall Medtronic TRILLIUM AFFINITY NT, Cardiotomy/Venous Reservoir (CVR) with Filter,with Trillium B 2018-01-16 United States USFDA
Recall of Device Recall Max Implant System 2017-06-16 United States USFDA
Recall of ABDOMINAL GYN PACK 2003-03-25 United States USFDA
Recall of Device Recall PowerPICC catheter 2017-12-28 United States USFDA
Recall of Device Recall Concorde Lift 2017-07-26 United States USFDA
Recall of Device Recall Concorde Lift 2017-07-26 United States USFDA
Recall of Device Recall cobas c 6000 MODULAR Series System e 601 2017-12-18 United States USFDA
Recall of Device Recall BrightView XCT 2017-12-15 United States USFDA
Recall of Device Recall Roche / Hitachi MODULAR Analytics Combination System 2017-12-18 United States USFDA
Recall of Device Recall cobas e 411 Immunoassay Analyzer 2017-12-18 United States USFDA
Recall of Device Recall 6.5" (17 cm) Smallbore Ext Set w/Remv MicroClave Clear, NanoClave TConnector, Clamp, Rotating Lue 2018-02-05 United States USFDA
Recall of Device Recall 6.5" (17 cm) Appx. 0.57 ml, Trifuse Ext Set w/3 MicroClave Clear, NanoClave TConnector 2018-02-05 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.

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