BfArM - Federal Institute for Drugs and Medical Devices

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Safety instruction for the CODMAN High Speed Drill System from Ethicon PDF, 427KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01680/05

MediTrade informs about the distribution of fakes PDF, 351KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03365/05

Exchange of all Nihon Kohden QI-403P Interface PDF, 56KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03363/05

Risks when using the povidon-iodine containing MiniCap/OptiCap disconnect caps from Baxter PDF, 173KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03332/05

Corrective action and Recall for Omni S system versions 2, 4 and 6 with CO-oximetry, Roche PDF, 104KB, Date: 10. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02832/05

Notification of issues with the Accura System for Blood Filtration from Baxter PDF, 183KB, Date: 09. January 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03034/05

Exatech recalls the Optetrak Cemented Finned Tibial Trays PDF, 44KB, Date: 03. January 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03407/05

The Mammendorfer Institut recalls the ECG Boy PDF, 28KB, Date: 02. January 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02357/05

Corrective action of Becton Dickinson for BD Logic glucometers PDF, 170KB, Date: 02. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03358/05

Corrective action of Abbott Medisense for Precision Xtra and Precision Xtra OK glucometers PDF, 123KB, Date: 02. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03354/05

Corrective action of Roche for Elecsys Troponin T PDF, 80KB, Date: 02. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03361/05

Safety risk in the wheel suspension of the three-wheeled chair Cheetah from R82 PDF, 169KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02987/05

Additional warning from Baxter BioScience for the product CoSeal PDF, 49KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03130/05

Risk of breakage in the backrest of the beds Arminia 2, Westfalia 3, Theutonia 3 and Fortuna from Burmeier PDF, 19KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02766/05

Corrective action of the ERBE Helix Hydro-Jet PDF, 77KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01470/05

Problems with the Neonatal Ventilator Baylog 8000plus from Dräger PDF, 63KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Reference 03343/05

Casters may break at Mobile Videocarts from Karl Storz PDF, 72KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00610/05

Recall of the Linvatec 300 Watt Xenon Light Source PDF, 88KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01388/05

Recall of the Vario Knee System Resection Guide Femoral Distal from Plus Orthopedics PDF, 23KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03151/05

Risk with the Prisma 2K from Siemens PDF, 59KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03010/05

Change of the German instruction for use for the TEC-5500 from Nihon Kohden PDF, 41KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02943/05

Boston Scientific recalls the Flextome Cutting Balloon™ Device Monorail™ Delivery System and Peripheral Cutting-Balloon Microsurgical Dilatation Device PDF, 178KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03220/05

Recall of Diamed for ID-Anti-Lea and AP P1-Lea-Leb-Lua-Lub-CtI PDF, 66KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03191/05

Corrective action and recall of Beckman Coulter for Cytomics FC 500 with CXP Software PDF, 307KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03250/05

Corrective action and recall of Immucor for the Galileo Analyzer PDF, 157KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03066/05

Advisory notice from Gambro for the Nephral ST dialyzers PDF, 61KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01899/05

Boston Scientific recalls Stainless Steel Greenfield™ Vena Cava Filter PDF, 783KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03189/05

Customer Information concerning the surgical lights Admeco-Lux PDF, 45KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03051/05

Recall of the product Removable T-Handle PDF, 42KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02884/05

Terumo Cardiovascular Systems recalls the Sarns Soft Flow Aortic Cannulae with Suture Flange PDF, 133KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02707/05