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Recall for CA 125II Reagent Lot 144 (ADVIA Centaur Systems), Siemens PDF, 29KB, File does not meet accessibility standards Date: 18. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04740/10

Lot Recall for GemStar pump sets, Hospira PDF, 119KB, File does not meet accessibility standards Date: 18. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04759/10

Corrective action for ADVIA Chemistry Systems Ethanol_2 Reagent, Siemens PDF, 24KB, File does not meet accessibility standards Date: 18. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04765/10

Follow-up Information for Corrective Action for UniCel DxC systems, Beckman Coulter PDF, 142KB, File does not meet accessibility standards Date: 17. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00256/10

Urgent Safety Notice for Leica Peloris™ Rapid Tissue Processor, Leica Biosystems Newcastle Ltd. PDF, 82KB, File does not meet accessibility standards Date: 17. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03394/10

Recall for carpal button screws, Small Bone Innovation International PDF, 102KB, File does not meet accessibility standards Date: 17. January 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02431/10

Urgent Safety Notice for Novocastra TTF-1 Primary Antibodies, Leica Biosystems Newcastle Ltd. PDF, 95KB, File does not meet accessibility standards Date: 17. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02854/10

Lot Recall for Provox Vega Voice Prosthesis, ATOS PDF, 213KB, File does not meet accessibility standards Date: 17. January 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04768/10

Recall for GastroSoft biliary-stents, OptiMed PDF, 165KB, File does not meet accessibility standards Date: 17. January 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04698/10

Corrective action/Recall for Stratus CS STAT Fluorometric Analyzer, Siemens PDF, 99KB, File does not meet accessibility standards Date: 14. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04840/10

Important Safety Notice for Focal®, Elekta CMS Software PDF, 40KB, File does not meet accessibility standards Date: 14. January 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02653/10

Safety Notice for Paradigm Veo insulin pumps, Medtronic PDF, 117KB, File does not meet accessibility standards Date: 14. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04749/10

Safety Notice for Babylog VN 500, Dräger PDF, 80KB, File does not meet accessibility standards Date: 14. January 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04800/10

Lot Recall for Renasys Port, Smith & Nephew PDF, 80KB, File does not meet accessibility standards Date: 14. January 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 04742/10

Safety Notice for Injectomat TIVA Agilia Syringe Pump, Fresenius Kabi PDF, 56KB, File does not meet accessibility standards Date: 12. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04813/10

Lot Recall for ReNu® Multi-Purpose Solution, Bausch & Lomb PDF, 92KB, File does not meet accessibility standards Date: 11. January 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 04770/10

Safety Notice concerning a problem with eNTEGRA and Xeleris Workstations, GE Healthcare PDF, 47KB, File does not meet accessibility standards Date: 11. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04688/10

Safety Notice: MR System Blower Box Installation, GE Healthcare PDF, 66KB, File does not meet accessibility standards Date: 11. January 2011 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 04682/10

Recall for Bicarbonate FS, DiaSys Diagnostic Systems PDF, 57KB, File does not meet accessibility standards Date: 11. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04804/10

Safety Notice: Swapped MR gradient cables, GE Healthcare PDF, 50KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 04649/10

Recall Information on certain Navigation software applications, Stryker PDF, 40KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04614/10

Lot Recall for Super Arrow-Flex® Percutaneous Sheath Introducer Set with Integral Hemostasis Valve / Side Port, Teleflex Medical PDF, 180KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04748/10

Lot Recall for Amplatzer Sizing Balloon II, AGA Medical Corp. PDF, 103KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04792/10

Safety Notice for MAGNETOM Systems, Siemens Healthcare PDF, 60KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 03891/10

Corrective Action/Recall for Sensors for Seronorm Trace Elements Serum Level 2, SERO PDF, 46KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03327/10

Lot Recall for FMS Intermediary Tube Sets for Fluid Management, DePuy Mitek PDF, 237KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04675/10

Safety Notice for Spectra Optia Apheresis System, CaridianBCT PDF, 87KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04637/10

Safety Notice for Licox CMP Tissue Oxygen Monitors, Integra LifeSciences PDF, 73KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04778/10

Important Information for Potassium liquirapid, HUMAN PDF, 77KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04434/10