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

15,394 results

Filter

Results per page: 10 20 30

Safety Notice for Newdeal Large Qwix Measurer, Newdeal SAS PDF, 172KB, File does not meet accessibility standards Date: 24. August 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02775/09

Recall for central venous catheter, Teleflex Medical PDF, 199KB, File does not meet accessibility standards Date: 24. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02918/09

Recall for GlucoTel blood glucose meter, BodyTel Europe GmbH PDF, 98KB, File does not meet accessibility standards Date: 24. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02798/09

Safety Notice for Argus Pro LifeCare, Schiller Medizintechnik GmbH PDF, 64KB, File does not meet accessibility standards Date: 24. August 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04768/08

Recall for Lightwave Suction Ablators, ConMed Linvatec PDF, 75KB, File does not meet accessibility standards Date: 21. August 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03004/09

Recall for Icelock Expulsion Valve 551, Össur hf. PDF, 52KB, File does not meet accessibility standards Date: 21. August 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02284/09

Recall for WATCHMAN® LAA Closure Delivery System, Atritech Inc. PDF, 552KB, File does not meet accessibility standards Date: 20. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02411/09

Corrective action for UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter PDF, 89KB, File does not meet accessibility standards Date: 20. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02984/09

Recall for Columbus gliding surface/tibial insert of the article NN340 and NN222, Aesculap AG PDF, 53KB, File does not meet accessibility standards Date: 20. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02898/09

Recall for Wiseguide™ Guide Catheters, Impulse™ and Expo™ Angiographic Catheters, Boston Scientific PDF, 81KB, File does not meet accessibility standards Date: 20. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02978/09

Safety Information for WATCHMAN LAA Closure Technology, Atritech Inc. PDF, 59KB, File does not meet accessibility standards Date: 19. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02373/09

Recall for TriniCLOT aPTT HS, Trinity Biotech PDF, 67KB, File does not meet accessibility standards Date: 18. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01747/09

Safety Notice for Thermo Scientific Microm STP 420D, Microm International PDF, 94KB, File does not meet accessibility standards Date: 18. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02179/09

Recall for Columbia CNA Agar with 5% Sheep Blood, Improved II, Becton Dickinson PDF, 20KB, File does not meet accessibility standards Date: 17. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02250/09

Safety Notice for SYNCHRON UniCel DxC Clinical Systems - Tube Assembly 142, Beckman Coulter PDF, 40KB, File does not meet accessibility standards Date: 17. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02839/09

Follow-up Notice for AED Plus Defibrillator, Zoll PDF, 130KB, File does not meet accessibility standards Date: 17. August 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00668/09

Safety Information for AvantGuard 1600 beds - AvantGuard Li160A, Hill-Rom PDF, 40KB, File does not meet accessibility standards Date: 17. August 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01209/09

Recall for Factor V Leiden Kit, Roche PDF, 37KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02619/09

Corrective action for HeartStart MRx, Philips PDF, 186KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02693/09

Safety Notice for Aesculap cementless Bicontact N stem size 9, Aesculap AG PDF, 64KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02733/09

Safety Notice for Separator 032 - Penumbra System, Penumbra Inc. PDF, 56KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02751/09

Recall for INNOTEST hPLAP, INNOGENETICS PDF, 46KB, File does not meet accessibility standards Date: 14. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02600/09

Recall for intragastric balloons HELIOSPHERE, HELIOSCOPIE PDF, 72KB, File does not meet accessibility standards Date: 13. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02265/09

Corrective Action for EasyLink Informatics System, Siemens Healthcare PDF, 24KB, File does not meet accessibility standards Date: 13. August 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02617/09

Recall for Stryker PainPump Catheters, Stryker GmbH PDF, 112KB, File does not meet accessibility standards Date: 13. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02602/09

Recall for Hintegra saw blade 60° AO-Synthes, Newdeal PDF, 164KB, File does not meet accessibility standards Date: 12. August 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02312/09

Recall for HemaCarotid Patch ultrathin knitted, InterVascular S.A.S. PDF, 73KB, File does not meet accessibility standards Date: 12. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02542/09

Safety Notice for Targon PFT System - KH 535 R, Aesculap PDF, 107KB, File does not meet accessibility standards Date: 12. August 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02791/09

Information for Super Elastic Self-Crimping Nitinol Piston, AUDIO TECHNOLOGIES PDF, 141KB, File does not meet accessibility standards Date: 11. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02249/09