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  • Device 3188
  • Manufacturer 465
  • Event 124969
  • Implant 1
Name Date Date initiated Country Source
Recall of Teicoplanin QMS Reagent 2013-07-09 France ANSM
Recall of Oxoid Legionella BCYE Growth Supplement 2013-12-26 France ANSM
Recall of Brahms Cyfra 21-1 Reagent Kryptor 2013-11-06 France ANSM
Recall of Selective supplement for Yersinia 2013-11-15 France ANSM
Recall of BRAHMS TRAK human Reagent KRYPTOR 2013-10-04 France ANSM
Recall of Oxoid disks for antimicrobial susceptibility testing AMP10 2013-07-18 France ANSM
Recall of HLA typing reagent Lambda 2014-11-13 France ANSM
Recall of Fluorobeads T 2014-12-23 France ANSM
Recall of ImmunoCAP ISAC Reagent sIgE 2014-10-23 France ANSM
Recall of QMS Reagent - Teicoplanin 2014-01-24 France ANSM
Recall of Oxoid Disks for Vancomycin (Bacteriology) Antimicrobial Susceptibility Testing 2014-01-30 France ANSM
Recall of Brahms Free Reagent b-HCG Kryptor CAL (Biochemistry) 2014-02-17 France ANSM
Recall of Reagent Oxoid Legionella pneumophila 2014-02-27 France ANSM
Recall of Brahms Free Reagent b-HCG Kryptor CAL 2014-03-07 France ANSM
Recall of Cell Trays Lambda Reagent 2015-06-10 France ANSM
Recall of Oxoid Legionella BCYE Growth Supplement 2015-02-11 France ANSM
Recall of Antibiotic Discs Ticarcillin - Clavulanic Acid 2015-02-13 France ANSM
Recall of Antibiotic Disorders CN10 Gentamicin 2015-04-09 France ANSM
Recall of Herniatex and Surgipatch Wall Rehabilitation Implants 2014-04-01 France ANSM
Recall of Tosoh Hemoglobin F A2 Control Set reagent 2009-05-14 France ANSM
Recall of Calibrators AIA-PACK PA 2009-05-15 France ANSM
Recall of Calibrator AIA-Pack Bhcg Calibrator Set 2011-11-21 France ANSM
Recall of Reagent Aia-Pack Prog Sample diluting solution 2011-01-11 France ANSM
Recall of Device Recall Introducer catheter. 2005-01-10 United States USFDA
Recall of TriniCLOT aPTT S reagent 2009-05-11 France ANSM
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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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