BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Search i

Search help

  • Enter one or more search terms in the search field. Upper and lower case are not relevant.
  • As soon as you have entered three letters in the search field, various search words will be suggested from which you can choose one.
  • If you are searching for a certain group of words, put these words in double quotes. The hits will then contain the words in the order you entered, e.g. "medicines for children".
  • Multiple search terms can also be combined with the Boolean operators AND and OR. When using the operator AND, the results contain the intersection of all search terms. When using the operator OR, the hits contain one of the search terms or only individual search terms. The result set is therefore significantly larger. Please note that these operators must be written in capital letters.
  • If you receive a (too) large number of hits as a result of your search, you can narrow it down by using filters. These filter options appear to the left of the search results and are subdivided into:

    • category (e.g. safety of medicinal products, medical devices, code systems)
    • format (e.g. download, risk information, DHPCs)
    • time interval (e.g. last 30 days, older than ...)
  • Selected filters can be removed individually or all at once ("Show all results").
  • By default, search results are sorted by relevance, but they can also be sorted chronologically ("Latest entries first" or "Oldest entries first").

Enter search term

15,399 results

Filter

Results per page: 10 20 30

Safety Notice concerning a corrective action of the Lifepak 500 automated external defibrillator, Medtronic Physio-Control PDF, 72KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02793/11

Recall of certain lots of the Trinity Biolox Delta liner and Corin Biolox Delta modular head, Corin Medical Ltd PDF, 806KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02602/11

Urgent Safety Notice for Varian High Energy Clinacs® and TrueBeam™ Systems, Varian medical systems PDF, 191KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02546/11

Safety information and corrective actions for Applix Smart and Applix Vision Nutrition Pumps with defined lot numbers, Fresenius Kabi PDF, 20KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02419/11

Corrective action for Access Immunoassay Systems and UniCel DxI Immunoassay Systems, Beckman Coulter PDF, 582KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02259/11

Safety Notice for GE Centricity™ Web, Software-Versions 3.0x, GE Healthcare PDF, 66KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02386/11

Safety Notice for Discovery VCT, RX VCT, STE, RX and ST PET/CT systems with Dimension console, GE Healthcare PDF, 37KB, File does not meet accessibility standards Date: 01. July 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02506/11

Corrective action of the Surgical Lighting and Media Systems Harmony LA, LC 500 and LA 700, Steris PDF, 185KB, File does not meet accessibility standards Date: 01. July 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01597/11

Recall of several reference and lot numbers of the Coronary Ostia Cannula, Terumo PDF, 45KB, File does not meet accessibility standards Date: 01. July 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02472/11

Recall of the surgical sutures Surgilon, Ticron and Sofsilk, Covidien PDF, 673KB, File does not meet accessibility standards Date: 01. July 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 02689/11

Lot Recall of the Silicone CTS ® (Close to Shaft) Cuff Adjustable Neck Flange Tracheostomy Tubes (Wire reinforced), Arcadia Medical Corporation PDF, 76KB, File does not meet accessibility standards Date: 30. June 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02635/11

Recall of the artificial urinary sphincter “AMS 800 Urinary Control System”, AMS PDF, 108KB, File does not meet accessibility standards Date: 30. June 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02142/11

Safety Notice for Savanah Bath Seats manufactured by Patterson Medical Ltd., RUSSKA PDF, 728KB, File does not meet accessibility standards Date: 30. June 2011 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02609/11

Corrective action for BD Microtrol Candida albicans, Becton Dickinson PDF, 54KB, File does not meet accessibility standards Date: 30. June 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02023/11

Lot Recall of the genitourinary graft Elevate Pelvic Floor Repair Systems with IntePro Lite, AMS PDF, 69KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02144/11

Urgent Safety Notice for ARIA™, Varian medical systems PDF, 323KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02391/11

Lot Recall for the Comprehensive Primary & Fracture Shoulder Stem Inserter, Biomet Orthopaedics PDF, 44KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02405/11

Recall for BOWA electro surgical units ARC 300 and ARC 350, BOWA PDF, 301KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00653/11

Recall for the Mantis Rod Inserter, Stryker Spine Bordeaux PDF, 33KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02728/11

Software error of cranial / ENT Navigation software, BrainLAB AG PDF, 236KB, File does not meet accessibility standards Date: 22. June 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02643/11

Potential pacing inhibition with PARADYM ICDs, Sorin Biomedica CRM S.r.I. PDF, 43KB, File does not meet accessibility standards Date: 22. June 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02002/11

Update of urgent safety information regarding Scorpio T72 Tibia Insert Trials, Stryker Orthopaedics PDF, 167KB, File does not meet accessibility standards Date: 22. June 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02776/10

Safety risk of Artiste digital linear accelerators with syngo® RT Therapist Version 4.1, Siemens Healthcare PDF, 92KB, File does not meet accessibility standards Date: 21. June 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02637/11

Recall of elastomeric AccuFlo infusion pumps, Medpro International Ltd PDF, 157KB, File does not meet accessibility standards Date: 21. June 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01529/11

Possible misassembled plugs in chargers for Echo-Screen / AccuScreen, Natus Europe PDF, 90KB, File does not meet accessibility standards Date: 20. June 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02432/11

Field safety notice concerning malfunction when using syngo plaza with version VA20, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 20. June 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02130/11

Possible potential interference of Methylene Blue and other vascular dyes with readings on CDI Monitoring Systems, Terumo CardioVascular Systems PDF, 179KB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02633/11

Refitting of Spacelabs Medical Capnography Module model 91517, Spacelabs Healthcare PDF, 38KB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02519/11

Lot recall of Hemochron Jr. PT Cuvettes, International Technodyne Corporation (ICT) PDF, 63KB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02213/11

Incorrect Gantry Angle in Focal Plan Review for XiO IMRT Plans, Elekta CMS PDF, 76KB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04098/10