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Safety Notice for the Discovery NM/CT 670 SPECT/CT and Discovery NM 630 SPECT Systems, GE Healthcare PDF, 30KB, File does not meet accessibility standards Date: 25. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 06607/12

Recall for the TPHA 100 Kit, Biomerieux PDF, 55KB, File does not meet accessibility standards Date: 25. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05762/12

Updated Safety Information for the clinical Chemistry Analyzers AU2700/AU2700 Plus and AU5400, Beckman Coulter PDF, 393KB, File does not meet accessibility standards Date: 24. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00389/12

Urgent Safety Notice for the MammoDiagnost DR with advanced stereo, Philips PDF, 28KB, File does not meet accessibility standards Date: 24. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for mammographic diagnostics
Reference 06614/12

Safety Notice concerning the Hand control of care bed model Westfalia-Klassik and bed insert model Lippe IV, Burmeier GmbH & Co. KG PDF, 40KB, File does not meet accessibility standards Date: 24. October 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 06344/12

Safety Notice for the DigitalDiagnost patient carriage, Philips PDF, 84KB, File does not meet accessibility standards Date: 24. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 06422/12

Safety Notice for the Liko® Sabina® and Capella™ Sit-to-Stand Mobile Lifts, Liko AB PDF, 390KB, File does not meet accessibility standards Date: 23. October 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 06511/12

Recall for the flexible Drills D3,2 x 149, Exatech Deutschland GmbH PDF, 44KB, File does not meet accessibility standards Date: 23. October 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06447/12

Recall for the Biatain Ag Filler/Cavity Foam Dressing, Coloplast A/S PDF, 69KB, File does not meet accessibility standards Date: 23. October 2012 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 06358/12

Recall for the Trabecular Metal™ Reverse Shoulder Instrumentation Liner Impactor, Zimmer Inc. PDF, 64KB, File does not meet accessibility standards Date: 22. October 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04790/12

Recall for aixstent Oesophagus, Leufen Medical GmbH PDF, 112KB, File does not meet accessibility standards Date: 22. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 05985/12

Safety Notice for Liko® Bathing Chair, Liko AB PDF, 62KB, File does not meet accessibility standards Date: 22. October 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 06294/12

Safety Notice for Tonometer Measuring Prisms, HAAG-STREIT AG PDF, 326KB, File does not meet accessibility standards Date: 22. October 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological diagnostics
Reference 00675/12

Recall for all 7-french-Endoprosthesis of old material (light blue), Wieser Medizintechnik und Geräte GmbH PDF, 145KB, File does not meet accessibility standards Date: 19. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 05968/12

Safety Notice concerning sat 805 and 816 pulse oximeters, Bitmos GmbH PDF, 67KB, File does not meet accessibility standards Date: 16. October 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06371/12

Corrective action of the HeartStart XL (M3735A) Defibrillator/Monitor battery M3561A, Philips Healthcare PDF, 67KB, File does not meet accessibility standards Date: 16. October 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06142/12

Recall for L2 poly liner, SMR Shoulder System, Limacorporate PDF, 55KB, File does not meet accessibility standards Date: 16. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06173/12

Lot specific recall of the Trilogy® Acetabular System Shell with Cluster Holes, Zimmer Inc. PDF, 49KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06272/12

Safety Notice for the Eclipse Treatment Planning System, Varian medical systems PDF, 335KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 06038/12

Safety Notice for Phaco I/A Tubing Cassette Quicksets, Carl Zeiss Meditec AG PDF, 24KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 05090/12

Recall for the Cancellous Bone Impactor, Synthes GmbH PDF, 546KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06246/12

Urgent Safety Notice for Actifuse, BAXTER PDF, 49KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - materials for implants
Reference 05767/12

Recall for Endoscopy suture anchors, SMITH & NEPHEW PDF, 55KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05472/12

Corrective action for ADVIA Centaur systems Calibrator B and ADVIA Centaur FSH assay on the ADVIA Centaur and ADVIA Centaur XP system, Siemens PDF, 143KB, File does not meet accessibility standards Date: 12. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05689/12

Safety Notice for the Brainlab Micro-Multileaf Collimator (MLC), Brainlab AG PDF, 675KB, File does not meet accessibility standards Date: 11. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 05736/12

Safety Notice concerning the Datex/GE compatible SpO2 sensor model S100A-300011, Solaris Medical PDF, 40KB, File does not meet accessibility standards Date: 11. October 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 02991/12

Lot Recall for ILLICO cannulated polyaxial screws, ALPHATEC SPINE PDF, 94KB, File does not meet accessibility standards Date: 10. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06262/12

Recall of Proximal Tibial Spacers made of Tilastan, Waldemar Link GmbH & Co. KG PDF, 221KB, File does not meet accessibility standards Date: 10. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05284/12

Corrective action for the UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter PDF, 100KB, File does not meet accessibility standards Date: 10. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05743/12

Safety Notice concerning Brilliance CT Big Bore with software versions 2.4.7 and 2.4.8, Philips Healthcare PDF, 105KB, File does not meet accessibility standards Date: 10. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06108/12