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Corrective action of the Picture Archiving and Communication System IMPAX DB Server, Agfa Healthcare PDF, 21KB, File does not meet accessibility standards Date: 04. September 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 04942/13

Urgent Safety Notice for the Philips MX 16-Slice, MX 4000, MX 4000 Dual and MX 6000 Dual 16 CT systems, Philips Healthcare PDF, 713KB, File does not meet accessibility standards Date: 03. September 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 04899/13

Recall for the Aequalis Reversed II and Reversed Fracture Impactors, Tornier SAS PDF, 1MB, File does not meet accessibility standards Date: 03. September 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04843/13

Lot Recall of the Violet Accelerator Free Nitrile Examination Gloves, HPC Healthline Ltd. PDF, 632KB, File does not meet accessibility standards Date: 03. September 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - auxiliary equipment
Reference 04840/13

Recall of SynCardia temporary Total Artificial Heart (TAH-t) with bi-leaflet mechanical valves, SynCardia Systems, Inc. PDF, 110KB, File does not meet accessibility standards Date: 03. September 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 04653/13

Corrective action for BacT/Alert® MP Culture Bottles, BioMerieux PDF, 59KB, File does not meet accessibility standards Date: 03. September 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 04554/13

Lot Specific Information about the Trabecular Metal™ Reverse Glenosphere Distractor, Zimmer PDF, 53KB, File does not meet accessibility standards Date: 02. September 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05052/13

Additional Recall for the Bioraptor, Osteoraptor and Twinfix Ultra Suture Anchors, SMITH&NEPHEW PDF, 117KB, File does not meet accessibility standards Date: 02. September 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 04655/13

Safety Notice for Trophy IRIX 65, IRIX 70, IRIX 708, NOVELIX 6510 and ORAMATIC 558, Carestream Health PDF, 370KB, File does not meet accessibility standards Date: 02. September 2013 Type: Customer information

Product group Radiological technology - radiological equipment for stomatological diagnostics
Reference 03392/13

Urgent Safety Information for the Inspira AIR™ Balloon Dilation System, Acclarent Inc. PDF, 59KB, File does not meet accessibility standards Date: 02. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 04894/13

Lot Recall of the Merit Performa® 5F Angiographic Cardiology Catheter, Merit Medical PDF, 277KB, File does not meet accessibility standards Date: 02. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02709/13

Safety Notice for the CARESTREAM DRX-Evolution X-ray systems, Carestream Health PDF, 14KB, File does not meet accessibility standards Date: 02. September 2013 Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 03941/13

Safey Notice for the BD Vacutainer® Multiple Sample Luer Adaptor, Becton Dickinson PDF, 39KB, File does not meet accessibility standards Date: 29. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion kits
Reference 03030/13

Corrective action for Vitek 2 Software version 6.01, BioMerieux PDF, 81KB, File does not meet accessibility standards Date: 29. August 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 03624/13

Corrective action for CoverStainer Slide Racks, Dako PDF, 1MB, File does not meet accessibility standards Date: 29. August 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 07310/12

Recall for the Oasys Midline Plates, STRYKER PDF, 16MB, File does not meet accessibility standards Date: 29. August 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02882/13

Recall of the Glidescope GVL and AVL reusable blades, Verathon PDF, 1MB, File does not meet accessibility standards Date: 29. August 2013 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 02850/13, 02851/13

Lot Recall of the H. Seidel Plug, 10mm DIA, Howmedica International S de R.L. PDF, 888KB, File does not meet accessibility standards Date: 29. August 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04565/13

Corrective Action for Padsy Flashlight Ergo, Medset PDF, 240KB, File does not meet accessibility standards Date: 28. August 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 04711/13

Corrective action for the Advia Centaur Folate Assay, Siemens PDF, 33KB, File does not meet accessibility standards Date: 28. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04484/13

Corrective Action for CSU 803x/603x, Dräger PDF, 961KB, File does not meet accessibility standards Date: 28. August 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04706/13

Lot Recall of the RIGIFLEX™ II Single Use Achalasia Balloon Dilator, Boston Scientific PDF, 34KB, File does not meet accessibility standards Date: 28. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03134/13

Recall for the T-Flex Aspheric intraocular lenses, Rayner PDF, 6MB, File does not meet accessibility standards Date: 28. August 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 03197/13

Recall of the Joline Acute Dialysis Catheters, Joline GmbH & Co. KG PDF, 1MB, File does not meet accessibility standards Date: 28. August 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00970/13

Corrective action for cobas b 123 Sensor Cartridge BG/ISE/GLU/LAC, Roche PDF, 144KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03755/13

Corrective action for GlucoMen LX Sensor test strips, EurimPharm PDF, 100KB, File does not meet accessibility standards Date: 27. August 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03844A/13

Corrective action for Dimension Vista® IRON Flex® reagent cartridge, Siemens PDF, 15KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06578/12

Corrective action for HemoCue Glucose 201 Microcuvettes, HemoCue PDF, 163KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03823/13

Lot Recall of the Cordis RADIALSOURCE™ Spring Wire Transradial Access Kit product, Cordis Corporation, Inc. and Greatbatch Medical PDF, 119KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03049/13