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Recall for specific Intraaortic Balloon Counterpulsation Catheters, Arrow International PDF, 483KB, File does not meet accessibility standards Date: 20. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04817/10

Safety Notice/Recall for the Bard Lifestent Vascular Stent System, Angiomed PDF, 471KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00019/11

Recall for MixMate 5353, Eppendorf AG PDF, 199KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00027/11

Safety Notice for the HeadFIX® system, Elekta PDF, 606KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03879/10

Safety Notice for PerOssal, aap Biomaterials PDF, 104KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03936/10

Corrective Action/Recall for ABX Micros 60, Horiba ABX SAS / Axonlab PDF, 121KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04839/10

Corrective Action for Synchron LX and UniCel DxC Clinical Systems – Operating Software, Beckman Coulter PDF, 34KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04775/10

Lot Recall for Ethilon, Ethibond, Mersilene and Perma-Hand Silk, Johnson & Johnson PDF, 121KB, File does not meet accessibility standards Date: 18. January 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 04835/10

Corrective Action for UniCel DxC Clinical Systems, Beckman Coulter PDF, 66KB, File does not meet accessibility standards Date: 18. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04758/10

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