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Recall for the Mutars knee system, Implantcast PDF, 153KB, File does not meet accessibility standards Date: 03. April 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01295/13

Urgent Safety Notice for the esophagus applicators, Eckert & Ziegler PDF, 96KB, File does not meet accessibility standards Date: 03. April 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
Reference 01174/13

Recall for the Vertebral Body Stent with Balloon, Synthes PDF, 83KB, File does not meet accessibility standards Date: 03. April 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01233/13

Recall for the Oxford Uni Toffee Hammer, Biomet PDF, 4MB, File does not meet accessibility standards Date: 02. April 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01571/13

Recall for the ALERE CHOLESTECH LDX ALT*AST CASSETTE, Alere San Diego PDF, 122KB, File does not meet accessibility standards Date: 02. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01511/13

Recall for ALERE CHOLESTECH LDX hsCRP CASSETTE, Alere San Diego PDF, 82KB, File does not meet accessibility standards Date: 02. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01508/13

Safety Notice for the DePuy ReClaim® Reamer Extension, DePuy PDF, 223KB, File does not meet accessibility standards Date: 02. April 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01232/13

Safety Notice concerning Digital Accelerators, Elekta PDF, 531KB, File does not meet accessibility standards Date: 02. April 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 05517/12

Safety Notice for the RayStation 2.0, 2.5 and 3.0, RaySearch Laboratories PDF, 216KB, File does not meet accessibility standards Date: 02. April 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 01025/13

Safety Notice for the DePuy Specialist 2 Intramedullary Rod (SP2 IM Rod) PDF, 319KB, File does not meet accessibility standards Date: 28. March 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01228/13

Recall for the Diacap Ultra Dialysis Fluid Filter, B. Braun Avitum AG PDF, 46KB, File does not meet accessibility standards Date: 28. March 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 00891/13

Safety Corrective Action concerning Cap Diphragm assemblies for use with 3100A or 3100B high frequency oscillatory ventilators, CareFusion PDF, 751KB, File does not meet accessibility standards Date: 28. March 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01334/13

Recall for two components of the AMS 800® Urinary Control System, American Medical Systems PDF, 607KB, File does not meet accessibility standards Date: 28. March 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 01201/13

Recall of the hip stem type ABG II, Stryker PDF, 2MB, File does not meet accessibility standards Date: 28. March 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03016/12

Lot recall of Reinforced Endotracheal tubes Murphy and Magil, Unomedical PDF, 1MB, File does not meet accessibility standards Date: 27. March 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01303/13

Safety Notice for the ExacTrac 6.0 patient positioning system (ExacTrac versions 6.0.1 and 6.0.2 only), Brainlab PDF, 518KB, File does not meet accessibility standards Date: 19. March 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00945/13

Safety Notice for the IntelliSpace Portal version 4.0.2, Philips Healthcare PDF, 247KB, File does not meet accessibility standards Date: 19. March 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 01095/13

Corrective Action for Access/Access 2 Immunoassay Systems, SYNCHRON LXi 725 Clinical System and the UniCel DxC 600i SYNCHRON Access Clinical System, Beckman Coulter PDF, 433KB, File does not meet accessibility standards Date: 19. March 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01024/13

Corrective action for ABX DIFFTROL, Axon Lab AG PDF, 1MB, File does not meet accessibility standards Date: 19. March 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 01094/13

Lot Recall for the Triathlon Baseplate Impactor/Extractor, Stryker Orthopaedics PDF, 215KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01276/13

Recall of two additional lots of Coseal Surgical Sealant, Baxter PDF, 209KB, File does not meet accessibility standards Date: 18. March 2013 Topics: Medical devices Type: Customer information

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

Recall of one lot of the Dilatator, De Bakey, Gebrüder Martin GmbH PDF, 211KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Medical instruments for use in humans - vascular surgery
Reference 01118/13

Recall for Legionella Test Kit, Thermo Fisher PDF, 22KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00953/13

Safety Corrective Action for Artis systems with the software Artis VC20x/VC21A/VD10x that have a DSA license installed, Siemens Healthcare PDF, 769KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 01089/13

Lot Recall for the RimCup Shells, Biomet Spain Orthopaedics S.L. PDF, 3MB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00622/13

Safety Notice for the application of DBS Lead Cups for implantable Deep Brain Stimulation Leads, Medtronic PDF, 173KB, File does not meet accessibility standards Date: 15. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 00665/13

Safety Corrective Action regarding the programmer Q-TECH Model 2020 and the subcutaneous defibrillator SQ-RX Model 1010, CAMERON HEALTH/BOSTON SCIENTIFIC PDF, 139KB, File does not meet accessibility standards Date: 15. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 01070/13

Safety Notice for the syngo.plaza SW version VA 20 with Mammography license, Siemens Healthcare PDF, 1MB, File does not meet accessibility standards Date: 15. March 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01011/13

Recall for IDM software method for EliA Rheumafactor IgM in Phadia® 2500/ Phadia® 5000 Systems, ThermoFisher PDF, 159KB, File does not meet accessibility standards Date: 15. March 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 00706/13

Extension of the Instructions for Use for the Medacta femoral stem, Medacta International SA PDF, 1MB, File does not meet accessibility standards Date: 15. March 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01140/13