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Safety Notice for the syngo® RT Therapist version 4.3, Siemens Healthcare PDF, 56KB, File does not meet accessibility standards Date: 08. May 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 01572/13

Corrective action for OpenGene® DNA Sequencing System MicroCel™ 500 and 300 Buffer Chamber, Siemens PDF, 38KB, File does not meet accessibility standards Date: 08. May 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 01901/13

Batch recall of Restylane SubQ Lido, Galderma PDF, 403KB, File does not meet accessibility standards Date: 08. May 2013 Type: Customer information

Product group Non-active implants - materials for implants
Reference 01442/13

Safety Notice for the VP1600 Still Capture System, ConMed Linvatec PDF, 50KB, File does not meet accessibility standards Date: 08. May 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 01463/13

Safety Notice for the BariAir™ Therapy System, ArjoHuntleigh PDF, 50KB, File does not meet accessibility standards Date: 07. May 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 02482/13

Lot Recall of the support ring – Megasystem-C® Tumor- & Revision Surgery, Waldemar Link PDF, 54KB, File does not meet accessibility standards Date: 07. May 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01658/13

Safety Notice for enteral feeding pumps Flocare® Infinity™, Nutricia Medical Devices PDF, 25KB, File does not meet accessibility standards Date: 07. May 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 06706/12

Recall of electrosurgery instruments ENDOPATH Probe Plus II Shaft, Ethicon PDF, 251KB, File does not meet accessibility standards Date: 07. May 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02349/13

Recall for Legionella GVPC Selective Medium, Oxoid PDF, 22KB, File does not meet accessibility standards Date: 07. May 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02093/13

Lot Recall of the endotracheal tubes for paediatrics, Vygon S.A. PDF, 24KB, File does not meet accessibility standards Date: 06. May 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 02430/13

Lot Recall for Sure-Pro® and Sure-Pro Ultra® Embryo Replacement Catheters, Smiths Medical PDF, 54KB, File does not meet accessibility standards Date: 06. May 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01716/13

Recall for the Zilver PTX Drug-Eluting Peripheral Stent, Cook Ireland Limited PDF, 23KB, File does not meet accessibility standards Date: 06. May 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 02316/13

Recall for the product ProcedurePak®, Mölnlycke Healthcare PDF, 24KB, File does not meet accessibility standards Date: 06. May 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 02440/13

Safety Notice for XVI R3.5, R4.0, R4.2, and R4.5, Elekta PDF, 193KB, File does not meet accessibility standards Date: 06. May 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00317/13

Safety Notice for the products Optima CT660, Brivo CT385, Discovery PET/CT 610 and Discovery PET/CT 710, GE Healthcare PDF, 62KB, File does not meet accessibility standards Date: 06. May 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 01848/13

Lot Recall for Maxcem Elite, KERR PDF, 144KB, File does not meet accessibility standards Date: 06. May 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 01098/13

Additional surgical safety advice to the PANTA® Arthrodesis Nail Surgical Technique, Newdeal SAS PDF, 3MB, File does not meet accessibility standards Date: 03. May 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02346/13

Safety Notice concerning a corrective action of the CyberKnife Iris Variable Aperture Collimator Option (excluding M6 Series), Accuray International Sàrl PDF, 56KB, File does not meet accessibility standards Date: 03. May 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 01501/13

Lot Recall for the Compression Screw (PeekPower Distal Radius Plate), ARTHREX PDF, 577KB, File does not meet accessibility standards Date: 03. May 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01590/13

Important Safety Notice for the YUNO Table Extension Device, Maquet Getinge Group PDF, 98KB, File does not meet accessibility standards Date: 03. May 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01960/13

Safety Notice for the XVI R3.5.1, R4.2.1 und R4.5.1, Elekta PDF, 193KB, File does not meet accessibility standards Date: 02. May 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 00317/13

Corrective actions required for synedra AIM (synedra View sub-module) and synedra View Professional, Synedra PDF, 47KB, File does not meet accessibility standards Date: 02. May 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01440/13

Safety Notice for Vitrea Enterprise Suite, Vitrea, VitreaAdvanced, VitreaCore (VitalConnect) und Vitrea fX, Vital Images PDF, 73KB, File does not meet accessibility standards Date: 02. May 2013 Type: Customer information

Product group Medical data processing (software) - software for diagnostic radiology
Reference 00658/13

Recall of the flexible handle with old design, Synthes GmbH PDF, 914KB, File does not meet accessibility standards Date: 02. May 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02343/13

Safety Notice for iPlan RT Dose version 4.0 or 4.1 (including all subversions), Brainlab AG PDF, 633KB, File does not meet accessibility standards Date: 02. May 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 02063/13

Recall / Stop of distribution of all AcrySof® CACHET® intraocular lenses, Alcon Pharma GmbH PDF, 221KB, File does not meet accessibility standards Date: 30. April 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 01885/13

Recall for the Oxoid Antimicrobial Susceptibility Testing Disc TZP 36 Piperacillin/Tazobactam, Oxoid PDF, 22KB, File does not meet accessibility standards Date: 30. April 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00704/13

Urgent Field Safety Notice concerning Otismed® Shapematch® Cutting Guides, Stryker PDF, 83KB, File does not meet accessibility standards Date: 30. April 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02082/13