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Recall for NOVOCART® 3D Pin FR736, Aesculap PDF, 70KB, File does not meet accessibility standards Date: 10. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03230/09

Safety Notice for WaveScan Offline Programming Module (OPM), AMO Germany GmbH PDF, 206KB, File does not meet accessibility standards Date: 09. September 2009 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02991/09

Safety Notice for Innova 2121IQ, 3131IQ, 2100IQ, 3100IQ and 4100IQ, GE Healthcare PDF, 68KB, File does not meet accessibility standards Date: 09. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03179/09

Safety Notice for Innova 2000, 3100 and 4100 cardiovascular X-ray systems, GE Healthcare PDF, 136KB, File does not meet accessibility standards Date: 09. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03173/09

Important Notice for Quick-Type TM for Lifematch TM Update CD, Tepnel Lifecodes Date: 09. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02924/09

Information for ReFacto AF Laboratory Standard, Wyeth PDF, 218KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02858/09

Corrective action for D.light operating lamps, DKL Chairs GmbH PDF, 99KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 01236/09

Safety Notice for Ventri, GE Medical Systems PDF, 48KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02977/09

Recall for 4.00 Direct measuring Gauges, Smith & Nephew PDF, 54KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02694/09

Safety Notice for Acrobat 2000, Ondal Industrietechnik GmbH PDF, 13KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02060/09

Recall for Neuron Delivery Catheter 0.053, Penumbra PDF, 90KB, File does not meet accessibility standards Date: 07. September 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02740/09

Recall of actuators in hospital beds of cerain serial numbers, Wissner-Bosserhoff PDF, 392KB, File does not meet accessibility standards Date: 07. September 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02772/09

Recall for CellSearch® Circulation Tumor Cell Kit, Ortho Clinical Diagnostics PDF, 114KB, File does not meet accessibility standards Date: 07. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03034/09

Safety Notice for HLA B27 FITC-Conjugated Monoclonal Antibody, One Lambda, Inc. PDF, 49KB, File does not meet accessibility standards Date: 07. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02947/09

Recall for QuantiFeron-TB Gold TB Antigen Tubes, Cellestis PDF, 130KB, File does not meet accessibility standards Date: 07. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02999/09

Recall for PediCap End-Tidal CO2 Detectors, Covidien PDF, 71KB, File does not meet accessibility standards Date: 03. September 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03090/09

Field Safety Notice concerning a problem with Prowess Panther Treatment Planning System, Prowess PDF, 179KB, File does not meet accessibility standards Date: 01. September 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02949/09

Recall of Impact attachment ND270Rfor pre-assembled Plasmacup® delta, Aesculap AG PDF, 64KB, File does not meet accessibility standards Date: 01. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03091/09

Recall of three lots of Laryngoscope Handles “Safescope”, Vygon PDF, 94KB, File does not meet accessibility standards Date: 31. August 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02951/09

Recall of several models and lot mumbers of the Arthro-Knife, ConMed Linvatec PDF, 486KB, File does not meet accessibility standards Date: 31. August 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02979/09

Important Notice regarding Stratus OCT™ Instrument and Review Software 6.0.0., Carl Zeiss Meditec PDF, 173KB, File does not meet accessibility standards Date: 31. August 2009 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02464/09

Recall for Auto D Dimer Kit, Trinity Biotech PDF, 135KB, File does not meet accessibility standards Date: 26. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03007/09

Information for K-Tips, Roche PDF, 22KB, File does not meet accessibility standards Date: 26. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02945/09

Information for cobas e 411 software, Roche PDF, 335KB, File does not meet accessibility standards Date: 26. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02864/09

Recall for Ultrapower Diamond Wheel burs, ConMed Linvatec PDF, 140KB, File does not meet accessibility standards Date: 26. August 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03013/09

Recall for Innofluor Certican Assay, Seradyn / Thermo Fisher Scientific PDF, 56KB, File does not meet accessibility standards Date: 26. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02856/09

Recall for Self Tapping Cancellous Screw, SMITH & NEPHEW PDF, 55KB, File does not meet accessibility standards Date: 25. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02695/09

Recall for Zimmer Alumina Ceramic Femoral Head, Zimmer Inc. PDF, 191KB, File does not meet accessibility standards Date: 25. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02822/09

Recall for SHER-I-SWIV and SHER-I-BRONCH, Teleflex Medical PDF, 527KB, File does not meet accessibility standards Date: 25. August 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02976/09

Safety Information for REMstar M Series Humidifier, Philips Respironics PDF, 2MB, File does not meet accessibility standards Date: 25. August 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02479/09