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Safety Information for Puma and Beatle power wheelchairs, Handicare PDF, 140KB, File does not meet accessibility standards Date: 23. November 2010 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03930/10

Battery Recall, Akkuplanet PDF, 59KB, File does not meet accessibility standards Date: 23. November 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 04253/10

Lot Recall for Feeding Tube with Luer Lock, Convatec PDF, 413KB, File does not meet accessibility standards Date: 23. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03613/10

Urgent Safety Information for the Intraaortic Balloon Counterpulsation Catheter, Arrow International PDF, 72KB, File does not meet accessibility standards Date: 22. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02334/10

Urgent Safety Notice for Escalon Vascular Access Device, Maquet PDF, 56KB, File does not meet accessibility standards Date: 22. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01935/10

Software Update for the STP 420D/ES Tissue Processor, Microm International (Thermo Fisher Scientific) PDF, 186KB, File does not meet accessibility standards Date: 22. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03155/10

Medical Device Alert, MHRA PDF, 199KB, File does not meet accessibility standards Date: 22. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03383/10

Safety Notice for Syngo Dynamics, Siemens PDF, 116KB, File does not meet accessibility standards Date: 22. November 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02739/10

Corrective action/Recall for Dimension Vista Gentamicin (GENT) Flex reagent cartridge, Siemens PDF, 271KB, File does not meet accessibility standards Date: 19. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04115/10

Urgent Safety Notice for the Hi-Art Treatment System, TomoTherapy Incorporated PDF, 101KB, File does not meet accessibility standards Date: 19. November 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04189/10

Safety Notice for Operation table top 1150.16B0, Maquet PDF, 102KB, File does not meet accessibility standards Date: 19. November 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04196/10

Lot Recall for Microseal Master Cone, SYBRON ENDO PDF, 75KB, File does not meet accessibility standards Date: 19. November 2010 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 03753/10

Corrective action for Behring Coagulation System BCS, Siemens PDF, 63KB, File does not meet accessibility standards Date: 18. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03972/10

Amended Information for the ASR Hip implant, DePuy PDF, 502KB, File does not meet accessibility standards Date: 18. November 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01977/08

Corrective Action for CELL-DYN Emerald, Abbott PDF, 169KB, File does not meet accessibility standards Date: 18. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04044/10

Recall for Scorpio Fixed Femoral A/P-Sizing Guide and Scorpio Adjustable Sizing Guide, Stryker Orthopaedics PDF, 457KB, File does not meet accessibility standards Date: 18. November 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03737/10

Safety Notice for CADD-Legacy® Duodopa® pumps, Smiths Medical ASD PDF, 26KB, File does not meet accessibility standards Date: 18. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03682/10

Recall for Access Total T4 Calibrators (Part no.: 33805, lot no.: 917074, 008534), Beckman Coulter PDF, 86KB, File does not meet accessibility standards Date: 15. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03463/10

Recall of several catalog numbers of Scorpio NRG 4:1 cutting blocks, Stryker Orthopaedics PDF, 31KB, File does not meet accessibility standards Date: 15. November 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03400/10

Follow-up/Updates for CellTracks AutoPrep System, Ortho-Clinical Diagnostics / Veridex PDF, 155KB, File does not meet accessibility standards Date: 12. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01979/10

Safety Notice for Ultraview SL 2200, 2400 and 2600 Monitore with Wireless-Option, Spacelabs Medical PDF, 78KB, File does not meet accessibility standards Date: 12. November 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03550/10

Lot Recall for BD 5 ml Plastipak Syringe Luer-Lok-Tip, Becton Dickinson PDF, 24KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04152/10

Corrective Action for Core TDM Multi-Calibrator, Part no.. ODC6411 (Lot no. 0021 and 0022), Beckman Coulter PDF, 91KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03461/10

Corrective Action for G-6-PDH Control, Trinity Biotech PDF, 391KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03963/10

Important Notice for XVI, Elekta Ltd. PDF, 240KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03226/10

Safety Notice for Sarns Ultrasonic Air Sensor-Cable, Terumo PDF, 144KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04001/10

Safety Notice for OEC 9800 and 9900 X-ray systems (C-Arm), GE Healthcare PDF, 52KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03750/10

Corrective action for Dimension Vista V-LYTE Standard A (K820), Siemens PDF, 572KB, File does not meet accessibility standards Date: 10. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03106/10

Corrective Action for Synchron CX4/5/7 CE, CX4/5/7 Delta and CX9 ALX Clinical Systems, Beckman Coulter PDF, 250KB, File does not meet accessibility standards Date: 10. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03916/10