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Corrective Action for Dimension® Phosphorus (PHOS) Flex® Reagent Cartridge, Siemens PDF, 54KB, File does not meet accessibility standards Date: 30. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00759/13

Corrective action for LifeCycle Prenatal Screening, PerkinElmer PDF, 491KB, File does not meet accessibility standards Date: 29. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00675/13

Corrective action for the Vitek 2 Piperacillin/Tazobactam Test, Biomerieux PDF, 34KB, File does not meet accessibility standards Date: 29. April 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01656/11

Femoral Cannula Recall, Edwards Lifesciences Services GmbH PDF, 108KB, File does not meet accessibility standards Date: 29. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02064/13

Urgent Recall of umpteen single use sterile feeding bottles, Beldico SA PDF, 420KB, File does not meet accessibility standards Date: 29. April 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - medico-mechanical devices
Reference 01975/13

Lot Recall of the Laryvox Duo Brush cleaning brush for voice prostheses, Andreas Fahl Medizintechnik-Vertrieb GmbH PDF, 362KB, File does not meet accessibility standards Date: 29. April 2013 Type: Customer information

Product group Orthopaedic / Rehabilitation technology - care of natural and artificial body orifices
Reference 01972/13

Lot Recall for the USS Low Profile Pedicle Screw, SYNTHES PDF, 25KB, File does not meet accessibility standards Date: 29. April 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01841/13

Recall for the Biosure Drivers and Biosure Ratched Drivers, Smith & Nephew PDF, 50KB, File does not meet accessibility standards Date: 29. April 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02052/13

Recall for Modular Analytics EVO, Roche PDF, 137KB, File does not meet accessibility standards Date: 26. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01223/13

Recall for the TRUE Dilatation™ Balloon Valvuloplasty Catheters, Loma Vista Medical PDF, 88KB, File does not meet accessibility standards Date: 26. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01512/13

Recall of reciprocating and oscillating saw blades manufactured by Synvasive Technology, Inc., Zimmer Surgical PDF, 113KB, File does not meet accessibility standards Date: 26. April 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02046/13

Recall for OneTouch®Verio® Blood Glucose Meters, Lifescan PDF, 58KB, File does not meet accessibility standards Date: 26. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01313/13

Recall for cobas 4800 system – z480 instrument, Roche PDF, 101KB, File does not meet accessibility standards Date: 26. April 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 01561/13

Corrective Action for MicroScan Microbiology Systems (listed below), Siemens PDF, 24KB, File does not meet accessibility standards Date: 25. April 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01290/13

Safety Notice for the Monaco RTP System, Elekta PDF, 108KB, File does not meet accessibility standards Date: 25. April 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00677/13

Lot Recall for the Latex-Free Extension Set with Locking Luer "T", Hospira PDF, 416KB, File does not meet accessibility standards Date: 25. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 00974/13

Safety Notice for the Paradigm Insulin Pump, Medtronic PDF, 199KB, File does not meet accessibility standards Date: 25. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01687/13

Recall for Accu-Chek Inform II Battery Packs, Roche PDF, 4MB, File does not meet accessibility standards Date: 25. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00296/10

Corrective action of the KLS Martin Double-TFT monitor support arm system, Gebrüder Martin GmbH & Co. KG PDF, 4MB, File does not meet accessibility standards Date: 25. April 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01188/13

Recall for the STERRAD 100S Cassette, Advanced Sterilization Products PDF, 45KB, File does not meet accessibility standards Date: 25. April 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 01569/13

Urgent Safety Notice for Vitrea CT Brain Perfusion 2D, Vital Images, Inc. PDF, 33KB, File does not meet accessibility standards Date: 25. April 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01735/13

Recall for Renovision-Nephrostomy-Sets, Urovision GmbH PDF, 39KB, File does not meet accessibility standards Date: 25. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01419/13

Safety Notice concerning the monitor carrier (VESA mounting plate) of the support arms, Richard Wolf PDF, 6MB, File does not meet accessibility standards Date: 24. April 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07057/12

Corrective action concerning Rad-8 pulse oximeters, Masimo PDF, 406KB, File does not meet accessibility standards Date: 23. April 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 01765/13

Expanded Recall for the products Lapra-TY™ II Clip, PDS™ II, Vicryl™, Vicryl™ Plus, Vicryl™ Mesh, Ultrapro™ and Ultrapro™ Plug, Johnson & Johnson PDF, 340KB, File does not meet accessibility standards Date: 23. April 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 00455/13

Lot Recall of the old design of the TM Ardis Inserter, Zimmer Inc. PDF, 107KB, File does not meet accessibility standards Date: 23. April 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06302/12

Recall for the Custom Procedure Trays containing 50 ml Luer Lock Syringes of the manufacturer Terumo, ArcRoyal PDF, 3MB, File does not meet accessibility standards Date: 23. April 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 01567/13

Corrective action of the syngo Workflow MLR using with “Portal Radiologist”, Siemens AG Healthcare PDF, 3MB, File does not meet accessibility standards Date: 23. April 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01717/13

Urgent Safety Infomation for Rigid Lenses, ESCAD PDF, 157KB, File does not meet accessibility standards Date: 23. April 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 05035/12

Corrective action for the Automated Hematology Analyzer, Sysmex PDF, 43KB, File does not meet accessibility standards Date: 22. April 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 01287/13