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

14,725 results

Filter

Results per page: 10 20 30

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

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