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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