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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

Corrective action for COBAS INTEGRA 400/400 plus systems, Roche PDF, 336KB, File does not meet accessibility standards Date: 20. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04263/07

Information for the Carendo Multi purpose Hygien Chair, Arjo PDF, 28KB, File does not meet accessibility standards Date: 20. December 2007 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03881/07

Information for the patient hoists Foldy, Torneo and Duo, Aktuelle Krankenpflege Systeme PDF, 1MB, File does not meet accessibility standards Date: 19. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03879/07

Corrective action for Dade Cardiac TL Assayed Cardiac Marker Control, ThermoFisher PDF, 34KB, File does not meet accessibility standards Date: 19. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04465/07

Recall of Complement Reagents (OWZD11), Dade Behring PDF, 59KB, File does not meet accessibility standards Date: 19. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04339/07

Recall of Universal and Ultraclean Electrodes, ConMed PDF, 70KB, File does not meet accessibility standards Date: 19. December 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04102/07

Recall of laryngeal masks, Besmed PDF, 24KB, File does not meet accessibility standards Date: 17. December 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04330/07

Recall of Cemento Fixx, OptiMed PDF, 103KB, File does not meet accessibility standards Date: 17. December 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04397/07

Information for ARCHITECT Folate assay, Abbott PDF, 3MB, File does not meet accessibility standards Date: 17. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01595/05

Corrective action for CRP LX and CRP HS to cobas 6000<cc> und cobas 6000<cce>, Roche PDF, 736KB, File does not meet accessibility standards Date: 17. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04300/07

Corrective action for Dimension clinical chemistry system Microalbumin Calibrator, Dade Behring PDF, 16KB, File does not meet accessibility standards Date: 17. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04415/07

Recall / Corrective action for Triage Meter Pro, Software Version 5.02, BIOSITE PDF, 123KB, File does not meet accessibility standards Date: 17. December 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04438/07

Information for Brilliance 6, 10, 16, 16P, 40, 64, BigBore und MX8000Dual v. EXP, Philips PDF, 35KB, File does not meet accessibility standards Date: 17. December 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04411/07

Recall of Singleday Infusor, Baxter PDF, 91KB, File does not meet accessibility standards Date: 17. December 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04366/07