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Recall for BA721 SKIN-GRFT CARRF/BA720R1:1.5STER, Aesculap PDF, 48KB, File does not meet accessibility standards Date: 23. September 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03425/10

Lot Recall for Hydrolift spine implants, AESCULAP PDF, 116KB, File does not meet accessibility standards Date: 23. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03178/10

Safety Notice for HeartMate II LVAS System Controller, Thoratec Corporation PDF, 248KB, File does not meet accessibility standards Date: 23. September 2010 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03165/10

Corrective action for Vitros Chemistry Products mALB Reagent Generation 2, 3 und 4, Ortho PDF, 268KB, File does not meet accessibility standards Date: 23. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03121/10

Safety Notice for AMPLATZER® Cardiac Plug, AGA Medical Corporation PDF, 96KB, File does not meet accessibility standards Date: 23. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03374/10

Recall for Architect Pre-Trigger Solution, Abbott PDF, 23KB, File does not meet accessibility standards Date: 20. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03089/10

Recall for Synchron Systems Modular Creatinine (CREm) Reagent Kits, Beckman Coulter PDF, 50KB, File does not meet accessibility standards Date: 20. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03013/10

Safety notice for Orbiter patient transfer system, Trumpf Medizin Systeme GmbH PDF, 94KB, File does not meet accessibility standards Date: 20. September 2010 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00500/10

Recall for defined series nos. of Dialog+, Diapact CRRT and Plasmat Futura, B. Braun Avitum AG PDF, 2MB, File does not meet accessibility standards Date: 20. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03325/10

Recall for TPHA 100, Biomerieux PDF, 58KB, File does not meet accessibility standards Date: 20. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03209/10

Information for GEM Check Coag Whole Blood Controls, Instrumentation Laboratory PDF, 276KB, File does not meet accessibility standards Date: 20. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02899/10

Recall of certain lots of the Easy Cyst Suprapubic Exchange Set for Children, Teleflex Medical PDF, 172KB, File does not meet accessibility standards Date: 20. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02068/10

Corrective action/Recall for IMMULITE 2000 3gAllergy Specific IgE Universal Kit, Siemens PDF, 24KB, File does not meet accessibility standards Date: 17. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01934/10

Safety Information for digital linear accelerators, Siemens PDF, 72KB, File does not meet accessibility standards Date: 17. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03173/10

Follow-up Information for Acute Care Troponin I TestPak on the Stratus CS STAT Fluorometric Analyzer, Siemens PDF, 42KB, File does not meet accessibility standards Date: 17. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01568/10

Lot Recall for Langston Dual-Lumen Pigtail Catheter, Vascular Solutions PDF, 352KB, File does not meet accessibility standards Date: 17. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03337/10

Safety Information for Instrument hoses of Planmeca Compact dental unit, PLANMECA OY PDF, 173KB, File does not meet accessibility standards Date: 17. September 2010 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02978/10

Recall for Orthopaedic bone-nailing compression screw / Orthopaedic instrument connecting screw, Stryker PDF, 27KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03201/10

Lot-Recall for Wingspan™ Stent System, BOSTON SCIENTIFIC PDF, 79KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03174/10

Chargen-Rückruf Wingspan™ Stent System, BOSTON SCIENTIFIC PDF, 93KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03174/10

Field Safety Notice concerning Navigation, StealthStation S7 Power Cord Retractor, Medtronic Navigation PDF, 2MB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02085/10

Safety Notice for Avance, Amingo and Aisys anaesthesia systems, GE Healthcare PDF, 125KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03232/10

Safety Notice for Pentax Light Sources BS-LH 1; BS-LH 2; BS-LL 1, Pentax PDF, 127KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03294/10

Safety Notice for Eclipse and RT Chart software, Varian Medical Systems PDF, 183KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03216/10

Field Safety Notice for Certain GE Responder 2000 Defibrillators, Cardiac Science Corporation PDF, 124KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02006/10

Follow-up Information for PLAC Test Reagent Kit Turbidimetric Immunoassay (TIA) Method, diaDexus PDF, 94KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04090/09

Safety Notice for Fresenius Medical Care bloodlines, Fresenius Medical Care PDF, 72KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02015/10

Safety Notice for Tonometer Measuring Prism, HAAG-STREIT AG PDF, 349KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02505/10

Customer Technical Bulletin concerning remote auto motions and differences on Clinac-software versions 6 and 7, Varian Medical Systems PDF, 624KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01973/10

Safety Notice for Powerheart, Cardio Vive and Responder Defibrillators, Cardiac Science PDF, 65KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04355/09