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Recall for "Cancellous Bone Screws and Gap Plate Screws", Stryker PDF, 240KB, File does not meet accessibility standards Date: 23. July 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02438/09

Recall for Restoration Modular Components, Stryker PDF, 240KB, File does not meet accessibility standards Date: 23. July 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02438/09

Recall for MDI Hybrid Implants with O-Ball Abutment, IMTEC PDF, 98KB, File does not meet accessibility standards Date: 22. July 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02557/09

Safety Notice for SynchroMed II Implantable Drug Infusion Pump - Model 8637, Medtronic PDF, 96KB, File does not meet accessibility standards Date: 22. July 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02461/09

Safety Notice for Arjo Carendo Multipurpose Hygiene Chair, Arjo Hospital Equipment AB PDF, 142KB, File does not meet accessibility standards Date: 22. July 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02212/09

Safety Notice for AV-Set Dialog, B. Braun PDF, 239KB, File does not meet accessibility standards Date: 21. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02547/09

Recall for LiNA Grey Shark and White Shark, LiNA Medical PDF, 127KB, File does not meet accessibility standards Date: 21. July 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02440/09

Safety Notice for LightCycler®-capillaries, Roche PDF, 26KB, File does not meet accessibility standards Date: 21. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02457/09

Recall for Hemoglobin F&A2 Control Set, TOSOH BIOSCIENCE PDF, 85KB, File does not meet accessibility standards Date: 20. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01701/09

Recall for chirurgical system da Vinci IS2000, Intuitive Surgical PDF, 86KB, File does not meet accessibility standards Date: 20. July 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02364/09

Safety Notice for GE Centricity PACS Software Versions 2.1.x and 3.0.x, GE Healthcare PDF, 90KB, File does not meet accessibility standards Date: 20. July 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00293/09

Safety Notice for GE Centricity PACS Software Versions 1.0.x and 2.0.x, GE Healthcare PDF, 85KB, File does not meet accessibility standards Date: 20. July 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00293/09

Safety Notice for Clearview HCG, Unipath PDF, 185KB, File does not meet accessibility standards Date: 17. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02273/09

Recall for Troponin I Test kits with rapid tests, HK Diagnostika PDF, 59KB, File does not meet accessibility standards Date: 17. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03365/08

Expanded Recall for ARCHITECT Reaction Vessels, Abbott PDF, 86KB, File does not meet accessibility standards Date: 17. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01620/09

Recall for Mini Crosser T-model and E-model scooters, Mini Crosser A/S PDF, 164KB, File does not meet accessibility standards Date: 17. July 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01998/09

Recall for ARCHITECT Total β-hCG Reagent, Abbott PDF, 28KB, File does not meet accessibility standards Date: 17. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02363/09

Safety Notice for Gemini TF 64 slice - Brilliance 64 CT scanners subcomponent, Philips PDF, 147KB, File does not meet accessibility standards Date: 15. July 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02460/09

Recall for Dimension Vista B2-Microglobulin Flex reagent cartridge, Siemens PDF, 43KB, File does not meet accessibility standards Date: 15. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01843/09

Recall for Dimension Vista Cystatin C Flex reagent cartridge, Siemens PDF, 46KB, File does not meet accessibility standards Date: 15. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01844/09

Recall for PSA Rapid Test, möLab PDF, 39KB, File does not meet accessibility standards Date: 15. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01840/09

Recall for test-kit PCT direct, BRAHMS Date: 15. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01999/09

Recall for Affinis stylus, Mathys PDF, 52KB, File does not meet accessibility standards Date: 15. July 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02024/09

Recall of certain lots of Celsite access portsystems with polyurethane catheter PDF, 63KB, File does not meet accessibility standards Date: 14. July 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02172/09

Recall for Compostop CS, the C5L, S5L and the C5LT apheresis disposables, Fresenius Kabi PDF, 57KB, File does not meet accessibility standards Date: 14. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02287/09

Information for PO5076A Cetrimide Agar, Oxoid PDF, 46KB, File does not meet accessibility standards Date: 14. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02106/09

Recall for Loglysis-catheter for intravascular treatment, OptiMed PDF, 112KB, File does not meet accessibility standards Date: 14. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02189/09

Field Safety Notice of the device Dynesis Top Loading Spacer Cutter PDF, 924KB, File does not meet accessibility standards Date: 14. July 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02133/09

Safety Notice for Lokomat system, Hocoma AG PDF, 123KB, File does not meet accessibility standards Date: 13. July 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02014/09

Recall for Immulite 2500 STAT iPTH, Siemens PDF, 68KB, File does not meet accessibility standards Date: 13. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02214/09