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Recall for Architect Trigger Level Sensors of Abbott PDF, 88KB, File does not meet accessibility standards Date: 22. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01015/07

Corrective action of the BEP 2000 / BEP 2000 Advance System from Dade Behring PDF, 46KB, File does not meet accessibility standards Date: 15. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01348/07

Software-upgrade of the Lifepak 20 defibrillator with software version 48 or 52 from Medtronic PDF, 67KB, File does not meet accessibility standards Date: 14. May 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01490/07

Information concerning the Diagnost 56, Diagnost 66 or Diagnost 76 Systems from Philips PDF, 46KB, File does not meet accessibility standards Date: 14. May 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02317/06

Information concerning the Polymobil III and Polymobil Plus systems from Siemens PDF, 38KB, File does not meet accessibility standards Date: 14. May 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01536/07

Recall of certain Fred Easy Defibrillators from Schiller PDF, 54KB, File does not meet accessibility standards Date: 11. May 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01521/07

Recall of the PET Esophageal and Pyloric/Colonic Balloon Dilators from ConMed PDF, 39KB, File does not meet accessibility standards Date: 11. May 2007 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01351/07

Information concerning the software iPlan Cranial 2.6, iPlan ENT 2.6, iPlan Stereotaxy 2.6 and iPlan Flow 2.6 from BrainLAB PDF, 81KB, File does not meet accessibility standards Date: 11. May 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01510/07

Information concerning the UV-Flash-Compact devices from Baxter PDF, 966KB, File does not meet accessibility standards Date: 10. May 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01586/07

Corrective action of the Coulter LH 780 Hematology Analyzers from Beckman Coulter PDF, 127KB, File does not meet accessibility standards Date: 10. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01575/07

Corrective action of the Coulter GENOS Hematology Analyzers from Beckman Coulter PDF, 57KB, File does not meet accessibility standards Date: 10. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01578/07

Corrective action of the Coulter LH 500 Hematology Analyzers from Beckman Coulter PDF, 116KB, File does not meet accessibility standards Date: 10. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01577/07

Corrective action of the Coulter LH 750 Hematology Analyzers from Beckman Coulter PDF, 126KB, File does not meet accessibility standards Date: 10. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01576/07

Corrective action of AxSYM Troponin I ADV, AxSYM CA125, AxSYM Folate and AxSYM Myoglobin from Abbott PDF, 490KB, File does not meet accessibility standards Date: 10. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01464/07

Recall of the Clearview Simplify D-Dimer from Unipath PDF, 63KB, File does not meet accessibility standards Date: 10. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00811/07

Recall of the Vitros Immundiagnostic Products Troponin I Reagent Packs from Ortho PDF, 149KB, File does not meet accessibility standards Date: 10. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01512/07

Recall of Human for Potassium Liquirapid PDF, 45KB, File does not meet accessibility standards Date: 08. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01299/07

Merckle Recordati GmbH informs about a recall PDF, 52KB, File does not meet accessibility standards Date: 08. May 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01104/07

Philips has issued an information that due to a software error of the HD11 Diagnostic Ultrasound System PDF, 32KB, File does not meet accessibility standards Date: 08. May 2007 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 01484/07

aap Biomaterials GmbH & Co. KG recalls certain lots of the EASYMIX Snorkel Revision PDF, 76KB, File does not meet accessibility standards Date: 08. May 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01346/07

Information from Siemens Medical Solutions PDF, 54KB, File does not meet accessibility standards Date: 08. May 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01333/07

Recall of the iView DAB Detection Kits from Ventana Medical Systems PDF, 53KB, File does not meet accessibility standards Date: 08. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01492/07

Recall by Endoart SA PDF, 57KB, File does not meet accessibility standards Date: 08. May 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01301/07

Information from Siemens Medical Solution of risks of softpot parameter PDF, 32KB, File does not meet accessibility standards Date: 04. May 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00028/07

Recall of the Dräger anaesthesia masks ComfortStar from Dräger PDF, 104KB, File does not meet accessibility standards Date: 04. May 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01433/07

GE Healthcare has issued an information about field corrective actions PDF, 55KB, File does not meet accessibility standards Date: 04. May 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01458/07

Recall of SeeOne 73 monthly contact lenses from Lenscare PDF, 38KB, File does not meet accessibility standards Date: 02. May 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 00905/07

Information concerning the shower-commode chairs model Bonn and Berlin from Rebotec PDF, 332KB, File does not meet accessibility standards Date: 02. May 2007 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02998/05

Information about the safe handling of the ThromCat Thrombectomy Catheter System from Kensey Nash PDF, 31KB, File does not meet accessibility standards Date: 02. May 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03721/06