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

15,399 results

Filter

Results per page: 10 20 30

Safety Notice for the OctoNova® Hemofiltration Device, Nikkiso PDF, 431KB, File does not meet accessibility standards Date: 02. March 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 04693/10

Recall of Intra Mobile Base, Planmeca PDF, 47KB, File does not meet accessibility standards Date: 02. March 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for stomatological diagnostics
Reference 06013/11

Recall of warming blanket of the Geratherm OP-Warming System, Geratherm Medical Diagnostic Systems PDF, 2MB, File does not meet accessibility standards Date: 01. March 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01019/12

Recall for Fluitest CREA PAP, of Analyticon PDF, 106KB, File does not meet accessibility standards Date: 01. March 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00765/12

Recall for chronOS Putty, MATHYS PDF, 358KB, File does not meet accessibility standards Date: 01. March 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00844/12

Safety Notice for the STERRAD® 200 System, ASP PDF, 46KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00477/12

Corrective action for ABL80 FLEX Analyzers configured with either FLEX or BASIC software, Radiometer Medical PDF, 37KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00377/12

Safety Notice for Varian Clinac® accelerators with Mark or Millennium MLC and BrainLAB m3 MLC, Varian medical systems PDF, 332KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 00911/12

Safety Notice for the S4 Cervical Occiput screw remover and removal shaft, Aesculap PDF, 557KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00926/12

Safety Information for the surgical systems da Vinci S, da Vinci Si and da Vinci Si-e, Intuitive Surgical PDF, 236KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00845/12

Corrective Action for CYTO-STAT tetraCHROME, Beckman Coulter PDF, 176KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00653/12

Korrekturmaßnahme für CYTO-STAT tetraCHROME, Beckman Coulter PDF, 36KB, File does not meet accessibility standards Date: 28. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00653/12

Lot Recall for the Biosure-HA Interference Screw, SMITH&NEPHEW PDF, 70KB, File does not meet accessibility standards Date: 28. February 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00847/12

Safety Notice for a peritoneal dialysis set with a catheter adaptor manufactured by Covidien and distributed by Baxter, Baxter PDF, 106KB, File does not meet accessibility standards Date: 28. February 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 05330/11

Safety Notice concerning a corrective action of the electrophysiology (EP) system Carto 3, Biosense Webster PDF, 667KB, File does not meet accessibility standards Date: 27. February 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 00850/12

Safety Notice for MultiDiagnost Eleva FD X-ray system, Philips PDF, 108KB, File does not meet accessibility standards Date: 27. February 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00843/12

Recall for the Columbus Revision knee endoprosthesis, Aesculap AG PDF, 101KB, File does not meet accessibility standards Date: 27. February 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 01001/12

Safety Notice for the BALTACCI Infusion Catheters, Balt Extrusion PDF, 796KB, File does not meet accessibility standards Date: 27. February 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00555/12

Recall for SafeSheath® CSG® Coronary Sinus Guide Braided Core Hemostatic Introducer, SafeSheath® Worley Telescopic Braided Series and Situs LDS 2 Lead Delivery System, GE Healthcare PDF, 70KB, File does not meet accessibility standards Date: 27. February 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05355/11

IFU upgrade of the MitraClip System, Abbott Vascular PDF, 492KB, File does not meet accessibility standards Date: 24. February 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 05617/11

Recall for the product AR ManoShield, Given Imaging PDF, 752KB, File does not meet accessibility standards Date: 24. February 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 04857/11

Safety Notice for implantable pulse generators for neurostimulation Eon, Eon Mini and Brio, St. Jude Medical PDF, 37KB, File does not meet accessibility standards Date: 24. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 05919/11

Safety Notice for Hamilton-G5 and Hamilton-S1 ventilators, Hamilton Medical PDF, 387KB, File does not meet accessibility standards Date: 24. February 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00841/12

Recall of mobile pneumatic drivers Freedom Driver System, Syncardia Systems Inc. PDF, 41KB, File does not meet accessibility standards Date: 24. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 05879/11

Recall of Companion 2 Drivers, Syncardia Systems PDF, 45KB, File does not meet accessibility standards Date: 23. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 06025/11

Recall of controller units of implantable HeartWare VAS, HeartWare Inc. PDF, 1MB, File does not meet accessibility standards Date: 23. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 05925/11

Recall of implantable pulse generators for neurostimulation Eon Mini and Brio, St. Jude Medical PDF, 39KB, File does not meet accessibility standards Date: 23. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 05924/11

Recall of implantable left ventricular assist device systems HeartAssist 5 LVAS, MicroMed Cardiovascular Inc. PDF, 636KB, File does not meet accessibility standards Date: 22. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 03533/11

Safety Information for the implantable left ventricular assist devices Incor, BerlinHeart PDF, 41KB, File does not meet accessibility standards Date: 22. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 04841/10

Recall of Software and Urgent Field Safety Notice according to HeartAssist 5 LVAS, MicroMed Cardiovascular Inc. PDF, 465KB, File does not meet accessibility standards Date: 22. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 00980/11