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Corrective action for Dimension® TACR Flex® Reagent Cartridges, Siemens PDF, 69KB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07258/12

Corrective action for androstenedione on Immulite® 1000, Immulite® 2000 and Immulite® 2000 XPi, Siemens PDF, 25KB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00022/14

Corrective action for Data-Cyte Plus 0,8 %, Medion Grifols Diagnostics AG PDF, 1MB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 07300/13

Corrective action for Cyclosporine (CSA) Flex reagent cartridge, Siemens PDF, 23KB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07513/13

Corrective action for AQURE V1.5.4, Radiometer PDF, 21KB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07240/13

Oertli Instrumente AG: Complete recall of the product Silicone application set, sterile for Opsia syringe PDF, 2MB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 07676/13

Safety Notice for the XIO RTP System, IMPAC Medical Systems PDF, 86KB, File does not meet accessibility standards Date: 15. January 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 07968/13

Corrective action for Instrument Manager Versions using Specimen Management or Rules-Only-packages, Data Innovations PDF, 69KB, File does not meet accessibility standards Date: 15. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07966/13

Corrective action for HER2 CISH pharmDX Kit, Dako PDF, 75KB, File does not meet accessibility standards Date: 15. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07617/13

Corrective action for Immulite 2000 and Immulite 2000 XPi, Siemens PDF, 36KB, File does not meet accessibility standards Date: 15. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07237/13

Corrective action for Analyzer 1.1.1 of the FluoroType MRSA-Kit, Hain Lifescience PDF, 201KB, File does not meet accessibility standards Date: 15. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07679/13

Urgent Field Safety Notice for the Femoral Arterial and Venous Cannula, Edwards Lifesciences PDF, 79KB, File does not meet accessibility standards Date: 15. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07891/13

Corrective action for BD BACTEC™ FX – Top Unit, Becton Dickinson PDF, 293KB, File does not meet accessibility standards Date: 14. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 07103/13

Corrective action for RAPIDPoint® 500 Systems, Siemens PDF, 31KB, File does not meet accessibility standards Date: 14. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07524/13

Lot Recall of the products Zimmer Periarticular Femoral Cond Buttress Plate, Zimmer Inc. PDF, 187KB, File does not meet accessibility standards Date: 14. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07997/13

Corrective action for RAPIDPoint® 400 Series, RAPIDPoint® 500 and RAPIDLab® 1200 Series Analyzers, Siemens PDF, 29KB, File does not meet accessibility standards Date: 14. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05828/13

Corrective action for LH 750 Hematology System and LH 780 Hematology System, Beckman Coulter PDF, 333KB, File does not meet accessibility standards Date: 14. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 07250/13

Corrective action for Vacuette 2 ml Glucomedics Tubes, Greiner Bio-One PDF, 510KB, File does not meet accessibility standards Date: 14. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 07376/13

Recall for the TWISTER™ PLUS Rotatable Retrieval Device, Boston Scientific (Distributor) / Horizons International Corporation PDF, 47KB, File does not meet accessibility standards Date: 14. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07179/13

Corrective action for Advia Chemistry Systems Advia 1200 and Advia 1650, Siemens PDF, 39KB, File does not meet accessibility standards Date: 13. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00016/14

Safety Notice for Infusion pump A707V / A708V, CODAN ARGUS AG PDF, 2MB, File does not meet accessibility standards Date: 13. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 00025/14

Safety Notice for the Super MultiVac 50 Coblation Wands, Arthrocare PDF, 2MB, File does not meet accessibility standards Date: 13. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00419/12

Another Safety Notice for the NOVO X 550 Dialysis Bed Chair, Likamed GmbH PDF, 2MB, File does not meet accessibility standards Date: 13. January 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 06105/13

Safety Notice for Echelon, ECHELON OVAL and OASIS MRI Systems, Hitachi Medical Corporation PDF, 254KB, File does not meet accessibility standards Date: 13. January 2014 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 07906/13

Lot Recall of the ATR 120 Autotransfusion Reservoir, Fresenius Kabi PDF, 124KB, File does not meet accessibility standards Date: 10. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - transfusion kits
Reference 07154/13

Urgent Safety Notice for the Essenta DR X-ray System, Philips Medical Systems PDF, 123KB, File does not meet accessibility standards Date: 10. January 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07903/13

Urgent Safety Notice for the device Navigation Compatible Accolade Broach Handle, Stryker Orthopaedics PDF, 98KB, File does not meet accessibility standards Date: 10. January 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07941/13

Urgent Safety Notice for the GEMINI TF Big Bore PET/ CT, Philips Healthcare PDF, 183KB, File does not meet accessibility standards Date: 10. January 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 07907/13

Batch recall of the products Rickham-style reservoir and Large Rickham-style reservoir, Integra LifeSciences Services PDF, 149KB, File does not meet accessibility standards Date: 09. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 07902/12

Urgent Safety Notice for the wheelchair model TMB, Trendmobil GmbH PDF, 1MB, File does not meet accessibility standards Date: 09. January 2014 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 06524/13