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Safety Notice concerning OEC devices, GE Healthcare PDF, 38KB, File does not meet accessibility standards Date: 14. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01203/08

Recall Kryosonde, H.P. Braem AG PDF, 93KB, File does not meet accessibility standards Date: 14. May 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01216/08

Recall of the Endoscopic Ligating Clip Applier (ELC), ConMed PDF, 186KB, File does not meet accessibility standards Date: 13. May 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00737/08

Preventive actions for syringe pumps type Module DPS, Fresenius Vial PDF, 55KB, File does not meet accessibility standards Date: 13. May 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00372/08

Information about iPlan RT Dose and VARiS, BrainLAB AG PDF, 96KB, File does not meet accessibility standards Date: 09. May 2008 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01377/08

Corrective action for Siemens N Latex CDT Kit, Siemens Healthcare Diagnostics PDF, 68KB, File does not meet accessibility standards Date: 09. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01502/08

Information about OEC devices, GE Healthcare PDF, 38KB, File does not meet accessibility standards Date: 09. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01202/08

Corrective action for Galileo Echo, IMMUCOR PDF, 212KB, File does not meet accessibility standards Date: 09. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01665/08

Corrective action of Lifepak 12 and Lifepak 20, Medtronic PDF, 23KB, File does not meet accessibility standards Date: 08. May 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01621/08

Safety Information about Blood Leak Detectors of single 4008 & 5008 dialysis system, Fresenius Medical Care PDF, 46KB, File does not meet accessibility standards Date: 08. May 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01312/08

Information about Dimension Clinical Chemistry System, Siemens PDF, 46KB, File does not meet accessibility standards Date: 08. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01622/08

Information about OEC products, GE Healthcare PDF, 54KB, File does not meet accessibility standards Date: 08. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01614/08

Information about DST-XL Gamma Camera, GE Healthcare PDF, 51KB, File does not meet accessibility standards Date: 08. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01615/08

Corrective action for Dimension ALDL Calibrator, Siemens Healthcare PDF, 53KB, File does not meet accessibility standards Date: 08. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01522/08

Recall for Dimension CTNI Flex reagent cartridge, Siemens Healthcare PDF, 50KB, File does not meet accessibility standards Date: 07. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01526/08

Information about CT scanners, Philips PDF, 311KB, File does not meet accessibility standards Date: 07. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01646/08

Recall for K-Wires, Abbott Spine PDF, 534KB, File does not meet accessibility standards Date: 07. May 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01680/08

Information about raised toilet seat “Soft”, Russka PDF, 55KB, File does not meet accessibility standards Date: 07. May 2008 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01083/08

Recall of BCI 3180 Pulse Oximeter, Smiths Medical PDF, 98KB, File does not meet accessibility standards Date: 05. May 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01169/08

Information about Mitsubishi Diamond Scan CRT displays, GE Healthcare PDF, 46KB, File does not meet accessibility standards Date: 05. May 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01089/07

Recall for "stainless steel arch wire natural upper", Highland Metals Inc. PDF, 33KB, File does not meet accessibility standards Date: 30. April 2008 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 01584/08

Recall of NaviStar® RMT ThermoCool® Irrigated Tip Catheter, Biosense Webster PDF, 40KB, File does not meet accessibility standards Date: 30. April 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00981/08

Information about CareVue Chart Patient Data Management System, Philips PDF, 109KB, File does not meet accessibility standards Date: 29. April 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00702/08

Information about Spectra Optia Apheresis System, Gambro PDF, 118KB, File does not meet accessibility standards Date: 29. April 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01523/08

Recall for Wallaby III Femoral Components, Zimmer PDF, 133KB, File does not meet accessibility standards Date: 25. April 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01348/08

Recall for Lactosorb Trauma Plate, Biomet PDF, 100KB, File does not meet accessibility standards Date: 25. April 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01336/08

Batch Recall for Heparin Adsorber, B.Braun PDF, 59KB, File does not meet accessibility standards Date: 25. April 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01353/08

Recall Trident® Acetabular cups, Stryker PDF, 417KB, File does not meet accessibility standards Date: 24. April 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00323/08

Recall MIH Mod Cup Inserter, Biomet PDF, 58KB, File does not meet accessibility standards Date: 24. April 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00429/08

Information for Definium 8000, GE Healthcare PDF, 52KB, File does not meet accessibility standards Date: 24. April 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01401/08