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Recall of the Cool-tip™ Ablation System from the company Tyco Healthcare Ltd. PDF, 55KB, File does not meet accessibility standards Date: 02. August 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01824/06

Recall of Model 7428 Kinetra from the manufacturer Medtronic PDF, 138KB, File does not meet accessibility standards Date: 02. August 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01922/06

Recall for the STA Cephascreen 4 reagent from the manufacturer Roche Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02073/06

Recall of special lots of the 8F Bard® Channel Steerable Sheath from the manufacturer Enpath Medical Incorporation PDF, 178KB, File does not meet accessibility standards Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02100/06

Recall of intrathecal catheters model 8731 and distal revision kits for intrathecal catheter model 8598 form the manufacturer Medtronic PDF, 82KB, File does not meet accessibility standards Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02116/06

Recall of the UROVACTM Bladder Evacuator from the manufacturer Boston Scientific Corporation PDF, 896KB, File does not meet accessibility standards Date: 28. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02027/06

Replacement of PEGA® CHARGER power supply devices from Pegasus PDF, 62KB, File does not meet accessibility standards Date: 25. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01612/06

Corrective action for Freelite Serum Free Light Chain Assays of The Binding Site PDF, 77KB, File does not meet accessibility standards Date: 25. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01866/06

Information for the Varian EXACT couch in combination with BrainLAB ExacTrac Robotics PDF, 204KB, File does not meet accessibility standards Date: 25. July 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01730/06

Recall of Vidas CA 15-3 from BioMerieux PDF, 172KB, File does not meet accessibility standards Date: 25. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01823/06

Recall of Microtrol Campylobacter jejuni from Becton Dickinson PDF, 32KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01821/06

Recall of GGT/IFCC Granulate System Kits from Roche PDF, 44KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02010/06

Recall of several batches of BD Difco Salmonella O and Shigella Antiserum Groups from Becton Dickinson PDF, 82KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01548/06

Corrective action and recall for the BCS Stirring Rack Unit of Dade Behring PDF, 87KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01526/06

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