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  • Device 788
  • Manufacturer 226
  • Event 124969
  • Implant 0
Name Date Date initiated Country Source
Recall of TI-CRON - BLUE BRAIDED POLYESTER FIBER 1998-05-11 Canada HC
Recall of ALARIS PATIENT CARE SYSTEM - ALARIS SERVER MOBILE SYSTEMS MANAGER 2010-09-07 Canada HC
Recall of CELL-DYN 4000 SYSTEM - CONTROL 2004-03-29 Canada HC
Recall of AW VOLUMESHARE 4 - SOFTWARE OPTIONS 2011-12-06 Canada HC
Recall of OBSERVA R02 BACT/ALERT 3D 2007-08-14 Canada HC
Recall of CATHCOR 2003-02-10 Canada HC
Recall of IMX SYSTEM - FOLATE REAGENTS 2004-01-08 Canada HC
Recall of LAP-BAND ACCESS PORT NEEDLES 2011-03-21 Canada HC
Recall of COBAS S201 SYSTEM POOLING AND DATA MANAGEMENT (PDM) V3.0.35 2015-04-27 Canada HC
Recall of T2 SCREWDRIVERS 2002-09-09 Canada HC
Recall of INSTATRAK 3500 SYSTEM 2007-04-04 Canada HC
Recall of VECTORVISION SKY - REFERENCE ARRAY 2011-08-02 Canada HC
Recall of IMMULITE 2000 SYSTEM - TROPONIN I ASSAY 2012-09-06 Canada HC
Recall of COBAS C 111 ALBT2 (TINA-QUANT) 2012-12-13 Canada HC
Recall of EPIPHANY PACK 2004-06-01 Canada HC
Recall of EPIC + VR ICD 2005-06-23 Canada HC
Recall of ANATOMICAL SHOULDER SYSTEM - RASP HANDLE 2015-03-23 Canada HC
Recall of ARCHITECT SYSTEM - ANALYZER - CLASS 2 2006-10-04 Canada HC
Recall of TDX SP POWER WHEELCHAIR 2012-03-29 Canada HC
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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.