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Recall for certain HLS Cannulae, MAQUET PDF, 470KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05972/12

Lot Recall for the Barrier Extremity Drape, Mölnlycke Healthcare AB PDF, 70KB, File does not meet accessibility standards Date: 28. September 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04943/12

Urgent Safety Notice for the VeriSuite 1.8, MEDCOM GmbH PDF, 45KB, File does not meet accessibility standards Date: 28. September 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 05677/12

Safety Notice for the oxygen concentrator model Permox and Permox SilentCare, Dräger Medical GmbH PDF, 279KB, File does not meet accessibility standards Date: 27. September 2012 Topics: Medical devices Type: Customer information

Product group Physical therapy - equipment for oxygen therapy
Reference 03423/12

Safety Notice concerning the Power Wheelchair “B400“ with ISO-Set and the ISO-Set, Otto Bock Mobility Solutions GmbH PDF, 99KB, File does not meet accessibility standards Date: 27. September 2012 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 06079/12

Urgent Safety Notice for the NANOS Femoral neck prosthesis, OHST Medical Technology PDF, 18KB, File does not meet accessibility standards Date: 27. September 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03625/12

Recall of batches of Angled Surecan needles, B. Braun Medical PDF, 4MB, File does not meet accessibility standards Date: 27. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 05473/12

Corrective action for Immulite 2000 / Immulite 2000 XPi EBV-EBNA IgG, Siemens PDF, 39KB, File does not meet accessibility standards Date: 27. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05925/12

Lot Recall for the Persona ™ Cemented Tibia Drill, Zimmer Inc. PDF, 54KB, File does not meet accessibility standards Date: 27. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05897/12

Safety Notice for the Volcano s5/s5i™ Imaging System, Volcano PDF, 290KB, File does not meet accessibility standards Date: 26. September 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05632/12

Lot Recall for the Flexible Drill D3,2 x 149, OHST Medical Technology PDF, 271KB, File does not meet accessibility standards Date: 26. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05960/12

Safety Notice for Vitrea and Vitrea Enterprise Suite, Vital Images PDF, 36KB, File does not meet accessibility standards Date: 26. September 2012 Topics: Medical devices Type: Customer information

Product group Medical data processing (software) - software for diagnostic radiology
Reference 05760/12

Corrective action for the Posterior Fluidics Module of the Stellaris PC Vision system, Bausch + Lomb PDF, 104KB, File does not meet accessibility standards Date: 26. September 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 05757/12

Safety Notice for the Mavig Portegra 2 systems, Siemens Healthcare PDF, 343KB, File does not meet accessibility standards Date: 25. September 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05901/12

Safety Notice for the Mobile Detector Holder for Digital Diagnost X-ray systems, Philips PDF, 97KB, File does not meet accessibility standards Date: 25. September 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 06023/12

Lot recall of INTERCEPT Plasma system, Cerus Corporation PDF, 89KB, File does not meet accessibility standards Date: 24. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - therapeutic apheresis procedures
Reference 05866/12

Safety Notice for Terumo® Advanced Perfusion System 1, Terumo Cardiovascular Systems PDF, 107KB, File does not meet accessibility standards Date: 20. September 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Corrective Action for ABL800 and ABL700, Radiometer PDF, 25KB, File does not meet accessibility standards Date: 20. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03242/12

Lot Recall for the SURGIFLO Hemostatic Matrix Kit, ETHICON PDF, 89KB, File does not meet accessibility standards Date: 20. September 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 05658/12

Corrective Action for ABX PENTRA ML, HORIBA PDF, 187KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05593/12

Lot Recall of an infusion extension line named “T-connector Luer-Lock”, Hospira PDF, 550KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 05721/12

Safety Notice for the Philips Essenta DR Compact, Philips Medical Systems PDF, 34KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 05065/12

Recall for the Inflation Device, B. Braun Melsungen AG PDF, 29KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03950/12

Urgent Safety Notice for Riata and Riata ST silicone insulated defibrillation leads, St. Jude Medical PDF, 609KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 05563/11

Safety Notice for the Integrated Module Housing, Spacelabs Healthcare PDF, 35KB, File does not meet accessibility standards Date: 18. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 05803/12

Corrective action for Immulite 2000 / Immulite 2000 XPi Troponin I, Siemens PDF, 62KB, File does not meet accessibility standards Date: 18. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05896/12

Lot Recall for the Sarns™ Antegrade Cardioplegia Cannula, Terumo Europe NV PDF, 54KB, File does not meet accessibility standards Date: 18. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03905/12

Recall for Osseotite® Tapered Certain® Implants, BIOMET 3i PDF, 42KB, File does not meet accessibility standards Date: 18. September 2012 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 05638/12

Lot Recall for Sarns High-flow Aortic Arch Cannulas and Sarns Flexible Arterial Cannulas, Terumo Europe NV PDF, 67KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03903/12

Recall for the SPIDER® Flexible Clip Applier, TransEnterix PDF, 47KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 05169/12