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

Recall for Bard Magnum Disposable Biopsy Core Needles, C.R. Bard PDF, 149KB, File does not meet accessibility standards Date: 02. November 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03881/09

Recall Morcellex Tissue Morcellator, Ethicon PDF, 132KB, File does not meet accessibility standards Date: 02. November 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03829/09

Safety Notice for Voluson E6 and Voluson E8 Diagnostic Ultrasound Systems, GE Healthcare PDF, 51KB, File does not meet accessibility standards Date: 30. October 2009 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03868/09

Lot Recall for Kryptonite Bone Cement, Doctors Research Group PDF, 79KB, File does not meet accessibility standards Date: 30. October 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03902/09

Recall for CROSSOVER™ Sheath Introducer, Cordis PDF, 86KB, File does not meet accessibility standards Date: 30. October 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03869/09

Recall for Komet bone milling cutter H162SL, Gebr. Brasseler PDF, 68KB, File does not meet accessibility standards Date: 29. October 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 03875/09

Safety Notice for Toppen 77, RPG Group PDF, 22KB, File does not meet accessibility standards Date: 29. October 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03326/09

Recall for Reflex Hybrid Screw Extractor Draw Rods, Stryker Spine Bordeaux PDF, 27KB, File does not meet accessibility standards Date: 29. October 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03802/09

Safety Notice for syngo Imaging XS in combination with „JPEG Compression” license, Siemens PDF, 198KB, File does not meet accessibility standards Date: 29. October 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03398/09

Recall for Equalizer™ Occlusion Ballon Catheter, Boston Scientific PDF, 75KB, File does not meet accessibility standards Date: 28. October 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03779/09

Safety Notice for R Series Defibrillator, Zoll PDF, 60KB, File does not meet accessibility standards Date: 28. October 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03747/09

Information for passive sling clips / Lifter of Arjo, Medibo and BHM, Medibo Medical N.V. PDF, 583KB, File does not meet accessibility standards Date: 28. October 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03828/09

Recall of Wallaby III revision tibial insert D-14, constrainde, Zimmer PDF, 78KB, File does not meet accessibility standards Date: 27. October 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03347/09

Safety Notice for FRED Easyport - Automated External Defibrillator, Schiller PDF, 219KB, File does not meet accessibility standards Date: 27. October 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00597/08

Recall for Synex II Modular Vertebral Body Replacement System, Synthes PDF, 166KB, File does not meet accessibility standards Date: 27. October 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03552/09

Safety Notice for syngo Imaging XS, Siemens PDF, 120KB, File does not meet accessibility standards Date: 27. October 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03274/09

Safety Notice for PowerHeart AED G3, Cardiac Science Corp. PDF, 90KB, File does not meet accessibility standards Date: 27. October 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00166/09

Recall of all Power Medical Interventions, Inc. Products, Covidien PDF, 239KB, File does not meet accessibility standards Date: 26. October 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03608/09

Recall port systems, Agency for Medical Innovations PDF, 97KB, File does not meet accessibility standards Date: 26. October 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03787/09

Recall for Universal Cables, ConMed Linvatec PDF, 154KB, File does not meet accessibility standards Date: 26. October 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03626/09

Recall for surgical handpieces PowerPro®, PowerProMax™ and Mpower™, ConMed Linvatec PDF, 181KB, File does not meet accessibility standards Date: 26. October 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03614/09

Recall for SKATER Single Step und Choice Lock TCD products, Angiotech-PBN Medicals PDF, 157KB, File does not meet accessibility standards Date: 21. October 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03421/09

Recall for EndoClamp Aortic Catheters, Edwards Lifesciences PDF, 142KB, File does not meet accessibility standards Date: 21. October 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03783/09

Recall for ONLINE TDM Gentamicin Assay, Roche PDF, 58KB, File does not meet accessibility standards Date: 21. October 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03636/09

Recall for Medena tapered suction tips, Astra Tech PDF, 85KB, File does not meet accessibility standards Date: 20. October 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03661/09

Safety Notice for MAMMOMAT Inspiration Biopsy Unit, Siemens PDF, 152KB, File does not meet accessibility standards Date: 20. October 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03635/09

Safety Notice for Allura Integris Systems with OMCP Generator, Philips PDF, 109KB, File does not meet accessibility standards Date: 20. October 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02424/08

Recall for ISKD Intramedullary Skeletal Kinetic Distractor, Orthofix PDF, 241KB, File does not meet accessibility standards Date: 20. October 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03809/09

Safety Notice for Galileo Echo, Immucor PDF, 96KB, File does not meet accessibility standards Date: 19. October 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03528/09