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Recall Difco Shigella Antiserum Poly Group B, Becton Dickinson PDF, 31KB, File does not meet accessibility standards Date: 18. January 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04614/07

Recall Immulite C-Peptide-Assays, Siemens PDF, 31KB, File does not meet accessibility standards Date: 17. January 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00041/08

Software update of M3170 IntelliVue Patient Link, Philips PDF, 112KB, File does not meet accessibility standards Date: 17. January 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04410/07

Recall Columbus Tibia Hemi Spacers, B. Braun Aesculap PDF, 34KB, File does not meet accessibility standards Date: 17. January 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04381/07

Urgent Safety Notice for VISX™ STAR™ excimer laser chair, Advanced Medical Optics PDF, 51KB, File does not meet accessibility standards Date: 17. January 2008 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 00075/08

Information for DigitalDiagnost, Philips PDF, 450KB, File does not meet accessibility standards Date: 17. January 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04353/07

Information for Mevatron, Primus Plus and Oncor Impression, Siemens PDF, 92KB, File does not meet accessibility standards Date: 17. January 2008 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00143/08, 00144/08

Information for ICD-models VITALITY HE, RENEWAL 3 and 4, Boston Scientific PDF, 108KB, File does not meet accessibility standards Date: 16. January 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01393/06

Information for Bravo® pH Capsule, Medtronic PDF, 282KB, File does not meet accessibility standards Date: 16. January 2008 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 04328/07

Recall Syva Emit® II Plus, Dade Behring PDF, 23KB, File does not meet accessibility standards Date: 15. January 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00148/08

Corrective action for CA 19-9 Kryptor Reagent, Brahms PDF, 53KB, File does not meet accessibility standards Date: 14. January 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03822/07

Recall Battery Packs for LifeVest Wearable Defibrillator, Medicor PDF, 91KB, File does not meet accessibility standards Date: 14. January 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04175/07

Recall Variant II Turbo Hemoglobin System, Bio-Rad PDF, 108KB, File does not meet accessibility standards Date: 14. January 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04195/07

Information for Clinic Information Center (CIC), GE Healthcare PDF, 347KB, File does not meet accessibility standards Date: 14. January 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00059/08

Recall BioBall ZrO2, Merete Medical PDF, 43KB, File does not meet accessibility standards Date: 11. January 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01885/07

Recall Pastorex™ Strep Test, Bio-Rad PDF, 35KB, File does not meet accessibility standards Date: 10. January 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04396/07

Recall Argoguide Hydrophilic Guide Wire, Argon PDF, 142KB, File does not meet accessibility standards Date: 08. January 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04092/07

Information for Cardiolab/Mac-Lab/ComboLab IT, GE Healthcare PDF, 55KB, File does not meet accessibility standards Date: 08. January 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04284/07

Recall ultrasound transducer, B-K Medical PDF, 38KB, File does not meet accessibility standards Date: 08. January 2008 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 04338/07

Information for the multiFiltrate dialysis system, Fresenius PDF, 36KB, File does not meet accessibility standards Date: 08. January 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04479/07

Information for HomeChoice and HomeChoice Pro, Baxter PDF, 40KB, File does not meet accessibility standards Date: 08. January 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04269/07

Corrective action and recall for FACSDiva Software, Becton Dickinson PDF, 34KB, File does not meet accessibility standards Date: 07. January 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04497/07

Recall for CHOOSTENT and HANAROSTENT, MTW PDF, 73KB, File does not meet accessibility standards Date: 03. January 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04265/07

Recall of the Anspach single-use cutting burrs, Anspach Effort PDF, 76KB, File does not meet accessibility standards Date: 02. January 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03694/07

Recall of Software application cards Model 8870BBG 01, Medtronic PDF, 86KB, File does not meet accessibility standards Date: 02. January 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 04557/07

Recall of CD Horizon Agile Device, Medtronic PDF, 91KB, File does not meet accessibility standards Date: 02. January 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04509/07

Information for Evolution beds, Hill Rom PDF, 234KB, File does not meet accessibility standards Date: 21. December 2007 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00587/07

Recall of VITEK 2 GP identification cards, BioMérieux PDF, 51KB, File does not meet accessibility standards Date: 21. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04519/07

Advisory Notice for O-ARM® Intraoperative Imaging Systems, Medtronic PDF, 26KB, File does not meet accessibility standards Date: 21. December 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04322/07

Information for PACS System EasyVision RAD Release 4.2 V2, Philips PDF, 449KB, File does not meet accessibility standards Date: 21. December 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04351/07