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Corrective Action for the Access-Folate-Calibrators, Beckman Coulter PDF, 58KB, File does not meet accessibility standards Date: 18. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05025/12

Recall for RTU-TdT-339, Leica Biosystems PDF, 2MB, File does not meet accessibility standards Date: 18. January 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07175/12

Corrective Action for IMMULITE / IMMULITE 1000 folic acid, Siemens PDF, 61KB, File does not meet accessibility standards Date: 18. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07498/12

Recall for the RUSCH Macintosh Laryngoscope Disp. Metallic Kit, Teleflex PDF, 62KB, File does not meet accessibility standards Date: 17. January 2013 Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 07994/12

Recall for Troponin I Schnelltest, Mexacare PDF, 114KB, File does not meet accessibility standards Date: 17. January 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 05249/12

Safety Notice for the Terumo® Advanced Perfusion System 1: Flow Module – “No Tubing” Error PDF, 179KB, File does not meet accessibility standards Date: 17. January 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07576/12

Lot Recall for the Coseal Surgical Sealant, Baxter PDF, 68KB, File does not meet accessibility standards Date: 16. January 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 00033/13

Recall for the Quadra Trial Broach, Medacta International SA PDF, 2MB, File does not meet accessibility standards Date: 16. January 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07843/12

Safety Notice for the product AutoTac Delivery Handle und AutoTac Titanium Starter Kit, BIOHORIZON IMPLANT SYSTEMS PDF, 34KB, File does not meet accessibility standards Date: 15. January 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 07542/12

Recall of certain Electrosurgery Disposable Active Electrodes and Accessories, ConMed Corporation PDF, 199KB, File does not meet accessibility standards Date: 15. January 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 08011/12

Safety Notice for the Terumo Advanced Perfusion System 1 / Flow Module, Terumo CVS PDF, 160KB, File does not meet accessibility standards Date: 15. January 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07577/12

Corrective Action for Haemonetics TEG-Analytical Software, Haemonetics PDF, 175KB, File does not meet accessibility standards Date: 15. January 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 06737/12

Safety Notice for Mobile Monitoring Gateway (MMG), Ascom AB PDF, 77KB, File does not meet accessibility standards Date: 15. January 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07785/12

Corrective Action for Olerup SSP HLA-typing kit DQB1-High, Olerup SSP AB PDF, 129KB, File does not meet accessibility standards Date: 14. January 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 07144/12

Recall for Remel Xpect Clostridium difficile Toxin A/B, Oxoid PDF, 23KB, File does not meet accessibility standards Date: 14. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06088/12

Corrective Action for VITROS Chemistry Products HPT Reagent, Ortho Clinical Diagnostics PDF, 92KB, File does not meet accessibility standards Date: 14. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06913/12

Safety Notice for the Terumo® Advanced Perfusion System 1, Terumo PDF, 171KB, File does not meet accessibility standards Date: 14. January 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07486/12

Safety Notice for the AdVance® XP Male Sling System, American Medical Systems Inc. PDF, 95KB, File does not meet accessibility standards Date: 14. January 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 03814/12

Recall for ARCHITECT HAVAb-IgG, Abbott PDF, 27KB, File does not meet accessibility standards Date: 11. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06089/12

Recall: TrachSeal Endotracheal & Tracheostomy Closed Suction Systems, Intersurgical Ltd. PDF, 77KB, File does not meet accessibility standards Date: 11. January 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07550/12

Safety Notice for the InterVapor System, Uptake Medical PDF, 100KB, File does not meet accessibility standards Date: 11. January 2013 Type: Customer information

Product group Physical therapy - others
Reference 07557/12

Safety Notice concerning Terumo Advanced Perfusion System 1, Terumo CVS PDF, 152KB, File does not meet accessibility standards Date: 11. January 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07490/12

Lot Recall for the Offset Tibial Tray Adaptor, Biomet PDF, 107KB, File does not meet accessibility standards Date: 11. January 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 06401/12

Recall for the Aorfix Endovascular Stent Graft, Lombard Medical PDF, 2MB, File does not meet accessibility standards Date: 11. January 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 06618/12

Safety Notice and Recall of Lithium Ion Polymer Batteries used as componets of Companion Driver Systems, Syncardia Systems Inc. PDF, 126KB, File does not meet accessibility standards Date: 11. January 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 07652/12

Recall for the Aqualiner Hydrophilic Guidewires, NIPRO Europe PDF, 880KB, File does not meet accessibility standards Date: 10. January 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 04864/12

Lot Recall for the RHK Short Hinge Assembly, Biomet PDF, 77KB, File does not meet accessibility standards Date: 10. January 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 07539/12

Safety Notice for the Kryptonite bone cement, DOCTORS RESEARCH GROUP PDF, 6MB, File does not meet accessibility standards Date: 10. January 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02843/12

Recall for Oxoid Legionella BCYE Growth Supplement, ThermoFisher PDF, 22KB, File does not meet accessibility standards Date: 10. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05927/12

Safety Notice for application and recall of DBS Extensions Kits PDF, 94KB, File does not meet accessibility standards Date: 09. January 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 07585/12