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Recall of Cordis 6 French Infiniti Selective Diagnostic Catheters PDF, 88KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01992/06

Recall of the Boston Scientific IQ Guide Wire PDF, 133KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01993/06

Recall of Expo™ und Impulse™ Angiographic Catheters from Boston Scientific PDF, 287KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02026/06

Recall of Omnitest plus Control control solution from Braun Melsungen PDF, 39KB, File does not meet accessibility standards Date: 21. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01296/06

Corrective action and recall of for the Advia 2110 Hematology System from Bayer Healthcare PDF, 94KB, File does not meet accessibility standards Date: 21. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01658/06

Recall of Carotid Wallstent™ Monorail™ carotid endoprosthesis from Boston Scientific PDF, 2MB, File does not meet accessibility standards Date: 21. July 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01990/06

Warning against condom special offers in the Internet PDF, 134KB, File does not meet accessibility standards Date: 20. July 2006 Topics: Medical devices Type: Customer information

Product group Contraception
Reference 01989/06

Recall of Lp(a) Calibrator from Wako Chemicals PDF, 53KB, File does not meet accessibility standards Date: 19. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01959/06

Recall of POLYSITE® venous access ports by Laboratoires Perouse PDF, 69KB, File does not meet accessibility standards Date: 19. July 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01886/06

Recall of C-Peptide Kits from Laison PDF, 44KB, File does not meet accessibility standards Date: 17. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01626/06

Recall of Turbiquant N Rheumatology Standard SL, N/T Rheumatology Control SL/1 and N/T Rheumatology Control SL/2 from Dade Behring PDF, 285KB, File does not meet accessibility standards Date: 17. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01765/06

Recall of the Vigilance monitors from Edwards Lifesciences Services PDF, 33KB, File does not meet accessibility standards Date: 17. July 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01979/06

Information for the textile stretcher Werolife 210090 from Wero PDF, 45KB, File does not meet accessibility standards Date: 17. July 2006 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01782/06

Recall of NC464 and NC468T ACETABULAR CUP SC by Aesculap PDF, 58KB, File does not meet accessibility standards Date: 14. July 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01970/06

Recall of screw implants by aap Implantate AG PDF, 56KB, File does not meet accessibility standards Date: 14. July 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01955/06

Recall of BD Vacutainer® Direct Draw Adaptors and BD Vacutainer® Luer Adaptors by Becton Dickinson PDF, 51KB, File does not meet accessibility standards Date: 14. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01889/06

Recall of Surgical Instrumentkit for THA with „Unique“ customized femoral stem from Scandinavian Customized Prosthesis PDF, 58KB, File does not meet accessibility standards Date: 14. July 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01547/06

Exchanges in artificial feet from College Park Industries PDF, 58KB, File does not meet accessibility standards Date: 11. July 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02386/04

Information for the hand-driven bike model Shark from Sunrise Medical PDF, 148KB, File does not meet accessibility standards Date: 11. July 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01758/06

Recall of the SynchroMed EL implantable programmable pumps from Medtronic PDF, 61KB, File does not meet accessibility standards Date: 07. July 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01278/06

Information for the LAP Dorado Laser System PDF, 47KB, File does not meet accessibility standards Date: 07. July 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01512/06

Corrective action and recall of FreeStyle Mini, FreeStyle Freedom and Freestyle from Abbott PDF, 303KB, File does not meet accessibility standards Date: 07. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01551/06

Information for the use of Hem-o-lok large clip from Teleflex PDF, 260KB, File does not meet accessibility standards Date: 06. July 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01589/06

Information for the CADD-Legacy Duodopa Pump, Model 1400 from Smiths Medical PDF, 24KB, File does not meet accessibility standards Date: 06. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01518/06

Information for the INSIGNIA and NEXUS pacemakers from Guidant PDF, 260KB, File does not meet accessibility standards Date: 06. July 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01794/06

Recall of the biopsy instruments Fischer Cone Biopsy Excisor from Apple PDF, 47KB, File does not meet accessibility standards Date: 05. July 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01116/06

Information for the use of the Ablatherm Integrating Imaging system, EDAP PDF, 78KB, File does not meet accessibility standards Date: 04. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01465/06

Information for the remote-controlled X-ray systems from Siemens PDF, 90KB, File does not meet accessibility standards Date: 04. July 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00144/06

Recall of UniCel DxC600/600i/800 Synchron Clinical Systems Operating-Software from Beckman Coulter PDF, 50KB, File does not meet accessibility standards Date: 03. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01529/06

Recall of the trimming handles 205530000, 205540000 and 205550000 from pfm PDF, 114KB, File does not meet accessibility standards Date: 03. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01284/06