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14,972 results

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Corrective action for Central Monitors model CNS-6201, NIHON KOHDEN Corporation PDF, 649KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03606/15

Corrective action for IPS e.max Ceram and related products, Ivoclar Vivadent AG PDF, 112KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 03820/15

Corrective action for the products VIVA II, PRISMA II and MELODY II (Sleep apnea devices), anamed GmbH & Co. KG PDF, 195KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03361/15

Recall for the Celsite® Access Ports, B. Braun Medical France PDF, 649KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03811/15

Important Safety Notice for Dräger monitor holders with AC2000, Dräger Medical GmbH PDF, 1MB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03627/15

Corrective action for the product AMICA Probe, HS Hospital Service SpA PDF, 2MB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02903/15

Corrective action for Telemetry Systems, NIHON KOHDEN Corporation PDF, 636KB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03631/15

Urgent Safety Notice for the EIT PLIF Shaver, EIT Emerging Implant Technologies GmbH PDF, 830KB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03757/15

Corrective Action for OxiMax™ N-65 Handheld Pulse Oximeters and OxiMax™ N-560 Pulse Oximeters, Covidien Deutschland GmbH PDF, 250KB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03040/15

Corrective action for the Digital Radiography X-Ray System DX-D 100 Type 5410 or DX-D 100 Wireless Type 5411, Agfa HealthCare NV PDF, 85KB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 03593/15

Recall of Alcon ACCURUS® STANDALONE VITREOUS PROBES, Alcon Pharma GmbH PDF, 159KB, File does not meet accessibility standards Date: 18. June 2015 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 03643/15

Corrective action for the RAPIDLab 1260 and RAPIDLab 1265 Blood Gas analyzers, Siemens Healthcare Diagnostics PDF, 218KB, File does not meet accessibility standards Date: 18. June 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03147/15

Corrective action for the Shiley™ Neonatal and Pediatric products, Covidien LLC PDF, 2MB, File does not meet accessibility standards Date: 18. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03134/15

Recall for Guide Wire 2.8mm, Length 180mm with Thread, Synthes GmbH PDF, 2MB, File does not meet accessibility standards Date: 18. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03835/15

Corrective action for optimys stems standard and lateral, Mathys Ltd. Bettlach PDF, 40KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02698/15

Recall for various orthopedic products, Biomet Orthopedics PDF, 261KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03197/15

Corrective action - Manufacturer IFU replacement for the VariLase® Endovenous Laser Fibers and Procedure Kits, Vascular Solutions Inc. PDF, 139KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - laser technology
Reference 02574/15

Recall for the product ProcedurePak®, Mölnlycke Health Care PDF, 75KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 03759/15

Boston Scientific: Corrective action for specific CLEARSIGN II Amplifiers, which are part of the LABSYSTEM PRO EP Recording System PDF, 229KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03678/15

Corrective action for the product Centricity PACS-IW with Universal Viewer, GE Healthcare Systems PDF, 230KB, File does not meet accessibility standards Date: 16. June 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 03506/15

Recall of the Surgical Incise Drape included in Shunt Sets, Fuhrmann GmbH PDF, 1MB, File does not meet accessibility standards Date: 16. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03780/15

Corrective action for Barco surgical displays, Barco PDF, 112KB, File does not meet accessibility standards Date: 16. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03485/15

Recall for the Osteotomy Guiding Device, DePuy Synthes PDF, 3MB, File does not meet accessibility standards Date: 16. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03459/15

Corrective action for the product Somatom Emotion 6 / 16, Siemens Shanghai Medical Equipment Ltd. PDF, 7MB, File does not meet accessibility standards Date: 16. June 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 03534/15

Corrective action for the WIZARD2 Gamma Counter, PerkinElmer PDF, 103KB, File does not meet accessibility standards Date: 16. June 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03100/15

Recall of the DLP® Femoral Arterial Cannula product and DLP® Femoral Cannula and Insertion Kits, Medtronic PDF, 33KB, File does not meet accessibility standards Date: 16. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03724/15

Recall for Covidien Devon™ Light Glove included in CeMed procedure packs, CeMed GmbH PDF, 168KB, File does not meet accessibility standards Date: 16. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03377/15

Corrective action for the ELI 380 electrocardiograph, Mortara Instrument, Inc. PDF, 122KB, File does not meet accessibility standards Date: 15. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03550/15

Safety Information for the S4C Occiput Torque Wrench F/Set Screw, Aesculap AG PDF, 677KB, File does not meet accessibility standards Date: 15. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03499/15

Recall for Target Coils, Stryker Neurovascular PDF, 29KB, File does not meet accessibility standards Date: 15. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03392/15