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14,979 results

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Corrective action for the product Rotavirus Positive Control, Coris BioConcept PDF, 230KB, File does not meet accessibility standards Date: 10. October 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05527/14

Corrective action for the ARCHITECT Total T3 Reagent Kit, Abbott PDF, 23KB, File does not meet accessibility standards Date: 10. October 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 05998/14

Recall for the clavicle plate, anterior, lateral, Königsee Implantate GmbH PDF, 39KB, File does not meet accessibility standards Date: 10. October 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03790/14

Corrective action for Radiolucent Bone Lever Retractor, Synthes GmbH PDF, 4MB, File does not meet accessibility standards Date: 09. October 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06383/14

Corrective action for Zimmer® Universal Power System Handpieces, Zimmer Surgical SA PDF, 1MB, File does not meet accessibility standards Date: 09. October 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 06307/14

Corrective action for the Dolphin Inflation device - Caliber Inflation Device, Perouse Medical PDF, 323KB, File does not meet accessibility standards Date: 09. October 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 06501/14

Urgent Safety Notice for the phenox p64 ® Flow Modulation Device, phenox GmbH PDF, 173KB, File does not meet accessibility standards Date: 09. October 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 01016/14

Urgent Safety Notice for the BeneHeart D1 Defibrillator/Monitor, Shenzhen Mindray Bio-Medical Electronics Co., Ltd. PDF, 166KB, File does not meet accessibility standards Date: 08. October 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06245/14

Urgent Safety Notice for SPIROTOME, biopsy instruments, Medinvents NV PDF, 392KB, File does not meet accessibility standards Date: 08. October 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - gynaecology
Reference 06452/14

Additional Information concerning Harmonie™, Dynamis™ und Gerialit™ Hospital beds, Hill-Rom PDF, 294KB, File does not meet accessibility standards Date: 08. October 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 02384/12

Corrective action concerning the cleaning instructions for AMPLITUDE orthopedic surgical instruments, Amplitude SAS PDF, 95KB, File does not meet accessibility standards Date: 08. October 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05372/14

Follow-Up Information concerning Ascenda™ Intrathecal Catheters / Revision Kit, Medtronic PDF, 123KB, File does not meet accessibility standards Date: 06. October 2014 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - drug pumps
Reference 04023/14

Corrective action for the Philips Expression Information Portal (IP5), Philips Medical Systems / Invivo Corp. PDF, 123KB, File does not meet accessibility standards Date: 06. October 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06210/14

Urgent Safety Notice for the Accu-Chek® Spirit Combo insulin pump, Roche Diagnostics Diabetes Care PDF, 6MB, File does not meet accessibility standards Date: 02. October 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 06264/14

Important Safety Notice for Leksell Gamma Knife® Perfexion™ - stereotactic surgery system, Elekta PDF, 146KB, File does not meet accessibility standards Date: 02. October 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 06366/14

Recall for Mölnlycke Health Care ProcedurePak®, Mölnlycke Health Care PDF, 85KB, File does not meet accessibility standards Date: 02. October 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03765/14

Urgent Safety Notice for Pronefro Therapy Chairs, Pronefro - Produtos Nefrológicos, S.A. PDF, 548KB, File does not meet accessibility standards Date: 02. October 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 05797/14

Recall for the OffRoad™ Re-Entry Catheter System, Boston Scientific PDF, 147KB, File does not meet accessibility standards Date: 01. October 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 06090/14

Corrective action for Ingenuity CT, Ingenuity Core and Ingenuity Core128 CT systems, Philips Healthcare PDF, 318KB, File does not meet accessibility standards Date: 01. October 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06335/14

Important Information for the product IMPAX EE R20 Release XIII, Agfa HealthCare PDF, 23KB, File does not meet accessibility standards Date: 01. October 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 06327/14

Corrective action for the CARESCAPE™ Monitor B850, B650 or B450, GE Healthcare PDF, 78KB, File does not meet accessibility standards Date: 01. October 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03316/14

Urgent Safety Notice for the Topcon Specular Microscope model SP-1P, Topcon Corporation PDF, 681KB, File does not meet accessibility standards Date: 30. September 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 05953/14

Urgent Safety Notice for the IntelliSpace Portal Software Versions 5 and 6, Philips Healthcare PDF, 364KB, File does not meet accessibility standards Date: 30. September 2014 Topics: Medical devices Type: Customer information

Product group Medical data processing (software) - data processing facilities for image processing
Reference 05338/14

Urgent Safety Notice for the paediatric endotracheal tube, Vygon PDF, 3MB, File does not meet accessibility standards Date: 30. September 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05430/14

Corrective action for the GMK Intramedullary Extension Rod 100 mm, Medacta International SA PDF, 1MB, File does not meet accessibility standards Date: 30. September 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06155/14

Important Safety Notice for the MultiDiagnost Eleva with Flat Detector system, Philips Healthcare PDF, 335KB, File does not meet accessibility standards Date: 29. September 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 06139/14

Corrective action for Precision 500D X-ray imaging systems with CRT monitor suspension, GE Healthcare PDF, 97KB, File does not meet accessibility standards Date: 29. September 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 05990/14

Urgent Safety Notice for Piezo Surgery Units Type “Piezomed SA-320”, W&H Dentalwerk Bürmoos GmbH PDF, 98KB, File does not meet accessibility standards Date: 29. September 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic therapeutic equipment
Reference 05964/14

Urgent Safety Notice for Camino® Intracranial Pressure Monitoring Kits, Integra PDF, 97KB, File does not meet accessibility standards Date: 26. September 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03914/14

Recall for the product ProcedurePak®, Mölnlycke Health Care PDF, 32KB, File does not meet accessibility standards Date: 26. September 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 06237/14