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 for Das gesunde Plus Hals & Rachenspray, Deutpharm PDF, 115KB, File does not meet accessibility standards Date: 06. January 2010 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 04228/09

Recall for Skin-Bond, SAUER CONTINENCE PDF, 33KB, File does not meet accessibility standards Date: 05. January 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02529/09

Information for the HM355S / HM340E Rotary Microtome, Thermo Fisher Scientific PDF, 184KB, File does not meet accessibility standards Date: 05. January 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04259/09

Recall for Nexgen Tibial Baseplate, Zimmer PDF, 431KB, File does not meet accessibility standards Date: 04. January 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04624/09

Lot Recall for Genos MC/MT Mini Distractors, GEBRÜDER MARTIN PDF, 121KB, File does not meet accessibility standards Date: 04. January 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 04595/09

Recall for Oxoid Brain Heart Infusion, Oxoid PDF, 40KB, File does not meet accessibility standards Date: 30. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04724/09

Corrective action for TriniCHECK Control Level 1 and TriniCHEK Control Level 2, Trinity Biotech PDF, 115KB, File does not meet accessibility standards Date: 30. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04687/09

Safety Notice for ARTISTE™ MV linear accelerators with syngo® RT Therapist, Siemens PDF, 111KB, File does not meet accessibility standards Date: 29. December 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04727/09

Corrective action of the AED 10 and MRL Jumpstart defibrillators, WelchAllyn PDF, 668KB, File does not meet accessibility standards Date: 29. December 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00646/09

Corrective action for optional NIBP units, installed in defibrillators cardioLife, Nihon Kohden PDF, 75KB, File does not meet accessibility standards Date: 29. December 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04709/09

Corrective action for the UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter PDF, 59KB, File does not meet accessibility standards Date: 29. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04773/09

Corrective action for Galileo Echo, Immucor PDF, 172KB, File does not meet accessibility standards Date: 29. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04547/09

Recall for searcher-cores, Richard Wolf GmbH PDF, 118KB, File does not meet accessibility standards Date: 28. December 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 04631/09

Safety Notice for ARTISTE™ digital linear accelerator, Siemens PDF, 597KB, File does not meet accessibility standards Date: 28. December 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04718/09

Safety Notice for Confirma, Inc.´s CADstream®, GE Healthcare PDF, 108KB, File does not meet accessibility standards Date: 28. December 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 04683/09

Corrective Action for Galileo Echo, Immucor PDF, 186KB, File does not meet accessibility standards Date: 22. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04378/09

Information for the monitor units Eclipse™, Varian PDF, 171KB, File does not meet accessibility standards Date: 22. December 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04623/09

Information for the Digital Image Capture System SDC HD 0240050888 and 0240050888i, Stryker PDF, 322KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04714/09

Information for TriniCHECK Control Level 3, Trinity Biotech PDF, 92KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04484/09

Recall of Male Swab, Roche PDF, 15KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04339/09