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

15,453 results

Filter

Results per page: 10 20 30

Safety Notice for the SEVEN and SEVEN Plus Continuous Glucose Monitoring Systems, Dexcom Inc. PDF, 222KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00406/11

Safety Notice for Carescape Monitor B850, GE Healthcare PDF, 48KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01296/11

Safety Notice for the device GE Centricity™ PACS, GE Healthcare PDF, 40KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04444/10

Corrective action and recall for the enGen Laboratory Automation System, Ortho PDF, 113KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00450/11

Expanded Safety Notice for BrightSpeed Excel / Edge / Elite Select and BrightSpeed Elite CT Systems, GE Healthcare PDF, 157KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00491/11

Safety Notice for BV Libra, BV Endura and BV Pulsera mobile X-ray systems, Philips PDF, 161KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00563/11

Safety Notice for PACS Workstation IDS7 version 12.2.3., SECTRA PDF, 23KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04731/10

Recall of Access Thyroglobulin Antibody II A32898 (Lot-No. 012741, 014751, 016551 and 016838), Beckman Coulter PDF, 33KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00514/11

Recall of GEM Premier 4000 Glucose and Lactate Sensors due to falsely positive results, Instrumentation Laboratory PDF, 101KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01188/11

Lot recall of DCI Dynamic Cervical Spine Implant, PARADIGM SPINE PDF, 67KB, File does not meet accessibility standards Date: 18. March 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01244/11

Recall of Alcohol pads and swabsticks, VWR International GmbH PDF, 1MB, File does not meet accessibility standards Date: 17. March 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 00585/11

Recall of cobas c pack CA (Lot-No. 630204-01 and 631376-01), Roche PDF, 83KB, File does not meet accessibility standards Date: 17. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00927/11

Safety Notice for analysers of CS-2x00i series because of erroneous results due to heparin interference, Sysmex PDF, 22KB, File does not meet accessibility standards Date: 16. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00741/11

Lot recall of Drehmomentschlüssel 10NM M.T-Griff, model number NE160R, Aesculap AG PDF, 117KB, File does not meet accessibility standards Date: 16. March 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00658/11

Problem with backup unit of CARDIOHELP-i, the manually operated CARDIOHELP Emergency Drive (REF: 70104.8002), MAQUET Getinge Group PDF, 1MB, File does not meet accessibility standards Date: 16. March 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01059/11

Error in German Translation of Combitube Instruction for Use, Covidien PDF, 100KB, File does not meet accessibility standards Date: 15. March 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04777/10

Corrective action for ABL90 Flex, Radiometer PDF, 49KB, File does not meet accessibility standards Date: 14. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00247/11

Safety Notice for EEG recorder NicoletOne® System, CareFusion PDF, 104KB, File does not meet accessibility standards Date: 14. March 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02542/10

Safety Notice for the device Monaco, Elekta CMS Software PDF, 58KB, File does not meet accessibility standards Date: 14. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04654/10

Recall of Rhino Fiberscope Sheath, Medical Technical Promotion GmbH PDF, 221KB, File does not meet accessibility standards Date: 14. March 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 00984/11

Safety Notice for the device XiO®, Elekta PDF, 112KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02672/10

Lot Recall for Dermabond Skin Adhesive, Ethicon PDF, 273KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00571/11

Recall for the DynaChip HLA Antibody Analysis System, Invitrogen PDF, 225KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00485/11

Safety Notice for the device XiO®, Elekta PDF, 114KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02699/10

Safety Notice: Incorrect FlexMaps on XVI, Elekta PDF, 291KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00029/11

Safety Notice for the Triathlon® PKR Instruments, PEG Drill, Stryker Orthopaedics Mahwah PDF, 435KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00566/11

Corrective action for Advia Clinical Chemistry Systems Ethanol Reagent, Siemens PDF, 35KB, File does not meet accessibility standards Date: 10. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04765/10

Lot Recall of the user-specific Foliodrape CombiSets for ophthalmologic surgery, Paul Hartmann AG PDF, 261KB, File does not meet accessibility standards Date: 10. March 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 00929/11

Lot Recall: Microlance 30 G Needles and Plastipak 1ml Syringe with Microlance 30 G Needle, Becton Dickinson PDF, 31KB, File does not meet accessibility standards Date: 10. March 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00754/11 - 00756/11

Urgent Safety Notice for Precedence and SKYLight Spect Systems, Philips PDF, 44KB, File does not meet accessibility standards Date: 10. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00359/11