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

Urgent Safety Notice for the Samaritan PAD SAM 300/300P public access defibrillators, HeartSine Technologies Ltd. PDF, 2MB, File does not meet accessibility standards Date: 05. November 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05995/12

Urgent Safety Notice for the TruSystem 5500 operating table system, TRUMPF Medizin Systeme GmbH + Co. KG PDF, 78KB, File does not meet accessibility standards Date: 05. November 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 06465/12

Urgent Safety Notice for Snowden-Pencer Tebbetts Fiber Optic Retractors, CareFusion PDF, 396KB, File does not meet accessibility standards Date: 02. November 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 06788/12

Urgent Safety Notice for PROCARE Monitors B20 or B40, Software Version VSP-A_1.10 (or earlier), GE Healthcare PDF, 60KB, File does not meet accessibility standards Date: 02. November 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06820/12

Field Safety Notice concerning AEROcheck®sat 805 and AEROcheck®sat 816 pulse oximeters, HUM PDF, 254KB, File does not meet accessibility standards Date: 02. November 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06456/12

Recall for PSX Proximate® Skin Staple Extractors, ETHICON Endo-Surgery PDF, 2MB, File does not meet accessibility standards Date: 02. November 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 06561/12

Update of the Instructions for Use for Dental Handpiece (ruixin) RXGBK, YUYAO RUIXIN MEDICAL APPLIANCE PDF, 70KB, File does not meet accessibility standards Date: 31. October 2012 Topics: Medical devices Type: Customer information

Product group Dental products - equipment
Reference 03904/12

Safety Information for the PARACHUTE Implant System, CardioKinetix Incorporated PDF, 749KB, File does not meet accessibility standards Date: 31. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 05591/12

Urgent Safety Notice for the MOBICATH™ Bi-Directional Guiding Sheath (small and large curve), Greatbatch, Ltd. and Biosense Webster Inc. PDF, 217KB, File does not meet accessibility standards Date: 31. October 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 06617/12

Safety Notice for the Essenta DR Compact, Philips Medical Systems PDF, 26KB, File does not meet accessibility standards Date: 31. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 06709/12

Lot Recall of Cannulated Screw, SYNTHES PDF, 321KB, File does not meet accessibility standards Date: 31. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06620/12

Corrective Action for IMMULITE / IMMULITE 1000 in combination with the IMMULITE Osteocalcin Control Module, Siemens PDF, 45KB, File does not meet accessibility standards Date: 31. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06249/12

Recall of the Hyperion Extension Sleeves 25 mm and 30 mm, Biomet PDF, 211KB, File does not meet accessibility standards Date: 30. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06732/12

Lot Recall for the Guide Extension Epoca, Synthes GmbH PDF, 70KB, File does not meet accessibility standards Date: 30. October 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06392/12

Corrective Action for IMMULITE ACTH Control Module, Siemens PDF, 36KB, File does not meet accessibility standards Date: 30. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06363/12

Recall for QFT Gold Tubes, QFT Gold Tubes High Altitude (HA), QFT Gold Single Patient Pack HA and QFT Gold Single Patient Pack, QUIAGEN PDF, 112KB, File does not meet accessibility standards Date: 30. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06350/12

Safety Notice for the Acuson X150 and Sonoline G40 ultrasound systems, Siemens PDF, 493KB, File does not meet accessibility standards Date: 29. October 2012 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 06460/12

Safety Notice for the Guide tube for segments and cervical sleeves, straight (a component of the Segmented Cervix Applicator set), Varian medical systems PDF, 339KB, File does not meet accessibility standards Date: 29. October 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
Reference 06254/12

Additional safety and warning information concerning InfectoDell for wart treatment, InfectoPharm Arzneimittel PDF, 66KB, File does not meet accessibility standards Date: 29. October 2012 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - ointments and gels
Reference 04016/12

Safety Notice for Centricity PACS, GE Healthcare PDF, 41KB, File does not meet accessibility standards Date: 29. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 06611/12

Corrective Action for Enzygnost F1+2 (monoclonal), Siemens PDF, 777KB, File does not meet accessibility standards Date: 29. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 06579/12

Corrective Action for Arkray D-Concept D-01, Arkray PDF, 341KB, File does not meet accessibility standards Date: 26. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03973/12

Safety Information for monopolar electrodes mentioned in table 1, Reger Medizintechnik GmbH PDF, 142KB, File does not meet accessibility standards Date: 26. October 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01016/12

Safety Notice concerning Mini C-arm models InSight2 and InSight FD, Hologic PDF, 101KB, File does not meet accessibility standards Date: 26. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - mobile radiological diagnostic facilities
Reference 06275/12

Corrective Action for IMMULITE / IMMULITE 1000 / IMMULITE 2000 / IMMULITE 2000 XPI in combination with the IMMULITE IGF–I Control Module, Siemens PDF, 38KB, File does not meet accessibility standards Date: 26. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06334/12

Recall for LightMix Kit HFE, TIB MOLBIOL PDF, 38KB, File does not meet accessibility standards Date: 26. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05707/12

Safety Notice for Seno Advantage versions 2.1 and 2.2, GE Healthcare PDF, 67KB, File does not meet accessibility standards Date: 26. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 06637/12

Urgent Safety Notice for care beds Amara and Amara-Tero, Stiegelmeyer GmbH & Co. KG PDF, 300KB, File does not meet accessibility standards Date: 25. October 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 06335/12

Corrective Action for StreamLAB Automation Solutions, Siemens PDF, 88KB, File does not meet accessibility standards Date: 25. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06595/12

Recall for the Expert Tibial Nail Protect, SYNTHES PDF, 516KB, File does not meet accessibility standards Date: 25. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06247/12