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

15,455 results

Filter

Results per page: 10 20 30

Safety Notice for the Eclipse™ Treatment Planning System, Eclipse™ Treatment Planning System PDF, 292KB, File does not meet accessibility standards Date: 17. August 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 05353/12

Lot Recall of the Hemorrhoidal Circular Stapler Proximate PPH (Product Code PPH01 and PPH03), Ethicon Endo-Surgery PDF, 106KB, File does not meet accessibility standards Date: 16. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 05171/12

Recall for Vital Signs enFlow IV Fluid Warmer Straps, GE Healthcare PDF, 55KB, File does not meet accessibility standards Date: 15. August 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 01870/12

Recall for Imager™ II Angiographic catheters and Imager™ II catheters used in urology, Boston Scientific PDF, 62KB, File does not meet accessibility standards Date: 15. August 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01961/12

Recall of HIP Stems packaged before February 2008, Wright Medical Technology PDF, 270KB, File does not meet accessibility standards Date: 14. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 04753/12

Safety Notice for Hospital Beds manufactured by the former company Arnold, Hill Rom PDF, 71KB, File does not meet accessibility standards Date: 14. August 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 05242/12

Safety Notice for the Respironics V60 ventilator, Philips PDF, 548KB, File does not meet accessibility standards Date: 14. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05216/12

Recall of all Softcup oesophagus stents, Micro-Tech Nanjing Co. Ltd. PDF, 52KB, File does not meet accessibility standards Date: 14. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 04545/12

Safety Information on Patient Labels for Zimmer Products manufactured before March 2010, Zimmer GmbH PDF, 178KB, File does not meet accessibility standards Date: 13. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05198/12

Safety Notice concerning Reprocessing Instructions for EndoWrist Instruments, Intuitive Surgical Inc. PDF, 163KB, File does not meet accessibility standards Date: 10. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04776/12

Safety Notice for the surgical lights Sim.LED 5000/7000, S.I.M.E.O.N. Medical GmbH & Co. KG PDF, 30KB, File does not meet accessibility standards Date: 09. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04956/12

Additional Information about the Lot Recall of Creatinine (CREA) Flex reagent cartridges, Siemens PDF, 77KB, File does not meet accessibility standards Date: 09. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05635/11

Urgent Safety Notice for the Digital Accelerator, Elekta PDF, 58KB, File does not meet accessibility standards Date: 09. August 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 04817/12

Recall for EBV EBNA-1-IgG-ELISA PKS medac, Medac GmbH PDF, 77KB, File does not meet accessibility standards Date: 09. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05046/12

Corrective Action for RIA FT3, Beckman Coulter PDF, 33KB, File does not meet accessibility standards Date: 08. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04651/12

Safety Information about the Auto-Fetch functionality of the Centricity PACS-IW system, GE Healthcare PDF, 31KB, File does not meet accessibility standards Date: 08. August 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05058/12

Safety Notice for syngo Dynamics Version 9.5, Siemens Healthcare PDF, 112KB, File does not meet accessibility standards Date: 08. August 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04712/12

Urgent Field Safety Notice to the examination system 3D Optical Coherence Tomography with the Software OCT Viewer, Topcon Europe Medical B.V. PDF, 96KB, File does not meet accessibility standards Date: 08. August 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological diagnostics
Reference 04721/12

Recall of several lots of the silicone oil RT SIL-OL 1000, Carl Zeiss Meditech AG PDF, 175KB, File does not meet accessibility standards Date: 08. August 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - liquid media for ophthalmological purposes
Reference 04662/12

Recall of several T-Piece Resuscitation Circuits, GE Healthcare Clinical Systems PDF, 92KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05080/12

Corrective Action for Dimension RxL – Reagent Management System (RMS) Power Cord Plug, Siemens PDF, 209KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04718/12

Corrective Action for ABL800 and ABL700, Radiometer PDF, 25KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04808/12

Safety Notice concerning shifted Dose for XiO Proton Spot Beams, Elekta PDF, 119KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 03756/12

Safety Notice for EndoWrist Hot Shears™ instruments, Intuitive Surgical® PDF, 272KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04624/12

Safety Notice for the Portnoy Ventricular Catheter, Integra NeuroSciences PDF, 87KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 05048/12

Lot Recall for Optipac Refobacin Bone Cement R, BIOMET PDF, 81KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - materials for implants
Reference 04819/12

Urgent Safety Notice for syngo.plaza, Siemens Healthcare PDF, 512KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 04703/12

Lot Recall for Calistar A and Calistar P, Promedon S.A. PDF, 42KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 04221/12

Corrective Action for Dimension Vista HCYS Flex Reagent Cartridge, Siemens Healthcare PDF, 25KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04664/12

Important Information Update regarding Eon model 65-3716, Eon Mini model 65-3788 and Brio model 65-6788, St. Jude Medical PDF, 76KB, File does not meet accessibility standards Date: 03. August 2012 Topics: Medical devices Type: Customer information

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