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Corrective Action für COBAS TaqMan MTB Test, Roche PDF, 107KB, File does not meet accessibility standards Date: 28. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07465/12

Recall für LIP W11049 Blood Agar No 2 + Horse Blood, Fannin / Oxoid / lip PDF, 273KB, File does not meet accessibility standards Date: 28. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00369/13

Recall of intraocular lenses “Ioflex Foldable Intraocular lenses”, Mediphacos Ltda (Belo Horizonte, Brazil) PDF, 15MB, File does not meet accessibility standards Date: 28. January 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 02014/11

Corrective action for the IGF-I assay of IMMULITE / IMMULITE 1000 / IMMULITE 2000 / IMMULITE 2000 XPi, Siemens PDF, 149KB, File does not meet accessibility standards Date: 28. January 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07260/12

Safety Notice for Video-Duodenoscope TJF-Q180V, Olympus PDF, 739KB, File does not meet accessibility standards Date: 25. January 2013 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 00239/13

Recall of the 1.6mm Guidewire, Extremity Medical PDF, 858KB, File does not meet accessibility standards Date: 25. January 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00071/13

Software Update for diagnostic devices ALLEGRO Topolyzer VARIO and WaveLight Oculyzer II, Alcon Pharma GmbH PDF, 126KB, File does not meet accessibility standards Date: 25. January 2013 Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological diagnostics
Reference 07796/12

Safety Notice for the Centricity PACS-IW system, GE Healthcare PDF, 60KB, File does not meet accessibility standards Date: 25. January 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 07589/12

Recall for CTAD Blood Collection Tubes, Becton Dickinson PDF, 36KB, File does not meet accessibility standards Date: 24. January 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 07307/12

Safety Notice concerning the Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall®, Multirall® and Masterlift® Systems, Liko PDF, 811KB, File does not meet accessibility standards Date: 24. January 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 00220/13

Safety Notice for the Peritoneal Dialysis Devices containing Quinton Beta Cap Adapter, Covidien PDF, 3MB, File does not meet accessibility standards Date: 24. January 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 06145/12

Synthes GmbH: Recall of the Hand Switch, for Electric Pen Drive PDF, 1MB, File does not meet accessibility standards Date: 24. January 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00349/13

Safety Notice for OEC Uroview X-Ray system, GE Healthcare PDF, 1MB, File does not meet accessibility standards Date: 24. January 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03227/06

Recall for TactiCath Quartz Catheters, Endosense PDF, 890KB, File does not meet accessibility standards Date: 23. January 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07743/12

Corrective Action for Phenobarbital_2, Siemens PDF, 41KB, File does not meet accessibility standards Date: 23. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07501/12

Corrective Action for CLINITEK Altas and Chek-Stix, Siemens PDF, 114KB, File does not meet accessibility standards Date: 23. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07481/12

Corrective action for Syva Emit tox Serum Calibrators, Siemens PDF, 22KB, File does not meet accessibility standards Date: 23. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07653/12

Corrective Action for ADVIA Centaur and ADVIA Centaur XP, Siemens PDF, 35KB, File does not meet accessibility standards Date: 23. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07277/12

Corrective action for Ciprofloxacin, Oxoid PDF, 21KB, File does not meet accessibility standards Date: 23. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07262/12

Recall for Emit 2000 Phenobarbital Assay, Siemens PDF, 55KB, File does not meet accessibility standards Date: 23. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07446/12

Corrective action for Creatinine PAP SL, SEPPIM PDF, 3MB, File does not meet accessibility standards Date: 22. January 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06688/12

Recall for Oxoid Antimicrobial Susceptibility Testing Discs FOX30 (Cefoxitin), ThermoFisher PDF, 22KB, File does not meet accessibility standards Date: 22. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06975/12

Recall for BD BBL Taxo XV Factor Strips, Becton Dickinson PDF, 51KB, File does not meet accessibility standards Date: 21. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07385/12

Recall for LIP W11050 Columbia Blood Agar, Fannin Limited PDF, 272KB, File does not meet accessibility standards Date: 21. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00207/13

Software Update required on all MobileDiagnost wDR x-Ray systems, Philips Medical Systems PDF, 32KB, File does not meet accessibility standards Date: 21. January 2013 Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00138/13

Safety Notice for the Brainlab Ultrasound Adapter BK Medical, Brainlab AG PDF, 772KB, File does not meet accessibility standards Date: 21. January 2013 Type: Customer information

Product group Radiological technology - navigation systems
Reference 07621/12

Recall: Vital-Port® Mini Titanium Detached Silicone Catheter Infusion Port, Cook Vascular Incorporated PDF, 2MB, File does not meet accessibility standards Date: 21. January 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 01598/11

Safety Notice for fT4-CTK kit, DiaSorin S.p.A. PDF, 562KB, File does not meet accessibility standards Date: 21. January 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07308/12

Safety Notice for Liaison Biotrin Parvovirus B19 IgM, DiaSorin S.p.A. PDF, 4MB, File does not meet accessibility standards Date: 21. January 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07622/12

Lot Recall for the Terumo Tubing Sets-sucker line, Terumo Europe NV PDF, 200KB, File does not meet accessibility standards Date: 18. January 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 06238/12