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Recall for REVISIO S Shells, AQ Implants GmbH PDF, 454KB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Non-active implants
Reference 04778/13

Lot Recall of the dialysis concentrate HC 43-90, Fresenius PDF, 2MB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04337/13

Lot Recall of proVencare accessory “J-tipped safety guidewires“, Fresenius Medical Care PDF, 2MB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04080/13

Safety Notice for the HL 30 pump consoles, Maquet Getinge Group PDF, 653KB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00522/13

Safety Notice for Artis zee systems equipped with a card collimator from a specific lot, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Radiological technology
Reference 00460/13

Lot Recall for the product Modus 2.0 Cranial Plate, MEDARTIS PDF, 70KB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 04941/13

Lot Recall of the AlboGraft Polyester Vascular Grafts, LeMaitre Vascular PDF, 3MB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Non-active implants
Reference 03398/13

Safety Notice concerning the revision of the Instruction for Use, Zimmer GmbH PDF, 27KB, File does not meet accessibility standards Date: 11. September 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 03179/11

Revised Safety Notice for the product NordiPen®, Novo Nordisk PDF, 1MB, File does not meet accessibility standards Date: 10. September 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - insulin pens and pen cannulas
Reference 03570/13

Recall of all lots of OF-B194 Gas/Water Feeding Valves, Pentax PDF, 35KB, File does not meet accessibility standards Date: 10. September 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 05021/13

Lot Recall of the Disposable Tube Set for Power Systems, Aesculap AG PDF, 116KB, File does not meet accessibility standards Date: 10. September 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03080/13

Lot Recall for the Vitoss Bioactive Bone Graft Substitute, STRYKER PDF, 65KB, File does not meet accessibility standards Date: 10. September 2013 Type: Customer information

Product group Non-active implants - materials for implants
Reference 04893/13

Updated Safety Notice for the Eon Mini and Eon Mini Charger, St. Jude Medical PDF, 115KB, File does not meet accessibility standards Date: 09. September 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 05251/13

Safety Notice concerning the walking aid Crocodile 3 from R82 A/S PDF, 66KB, File does not meet accessibility standards Date: 09. September 2013 Type: Customer information

Product group Orthopaedic / Rehabilitation technology - daily living aids
Reference 05089/13

Safety Notice concerning the electric drive max2, AAT Alber Antriebstechnik GmbH PDF, 72KB, File does not meet accessibility standards Date: 09. September 2013 Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 03646/13

Corrective action for Microscan® Microbiology Systems regarding Microscan Synergies plus® and rapID/S plus Gram Negative Panels, Siemens PDF, 159KB, File does not meet accessibility standards Date: 09. September 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05265/13

Corrective action for XLD Agar, bioMérieux PDF, 167KB, File does not meet accessibility standards Date: 09. September 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 04664/13

Urgent Safety Notice for the Tec 6 and Tec 6 Plus Vaporizers, GE Healthcare PDF, 131KB, File does not meet accessibility standards Date: 06. September 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05268/13

Follow-up Information for the Homechoice Cycler Sets, Baxter PDF, 302KB, File does not meet accessibility standards Date: 06. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 02409/12

Corrective action for ABX Pentra Calcium CP, Horiba PDF, 397KB, File does not meet accessibility standards Date: 06. September 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05217/13

Lot Recall of the Syramed syringe pump infusion line, Fresenius Kabi PDF, 80KB, File does not meet accessibility standards Date: 06. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 04702/13

Corrective action for BEP III with Software BESX 5.0.1, 5.1 and 5.1.1, Siemens PDF, 73KB, File does not meet accessibility standards Date: 06. September 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 03908/13

Recall for safety cannulas of the type SeldiSAFE, Vygon PDF, 38KB, File does not meet accessibility standards Date: 05. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03035/13

Lot Recall for the Viscoject™ 2.2 Injector Set, Viscoject™ 1.8 Cartridge Set and Phaco Tips and Sleeves, Medicel AG PDF, 15KB, File does not meet accessibility standards Date: 05. September 2013 Type: Customer information

Product group Medical instruments for use in humans - eye surgery
Reference 04721/13

Lot Recall for the Swiss Bimanual / Monomanual I/A Systems, Medicel AG PDF, 16KB, File does not meet accessibility standards Date: 05. September 2013 Type: Customer information

Product group Medical instruments for use in humans - eye surgery
Reference 04720/13

Corrective action for Emit® 2000 Phenobarbital Assay, Siemens PDF, 23KB, File does not meet accessibility standards Date: 05. September 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05131/13

Urgent Safety Notice for Centricity PACS RA1000 Workstation, GE Healthcare PDF, 91KB, File does not meet accessibility standards Date: 05. September 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 04549/13

Urgent Safety Notice for the Advantx and Innova Cardiovascular X-ray imaging systems, GE Healthcare PDF, 107KB, File does not meet accessibility standards Date: 04. September 2013 Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 05173/13

Batch Recall of GENESIS™ II Posterior-Stabilized Inserts and Mobile Bearing Inserts, Smith & Nephew PDF, 64KB, File does not meet accessibility standards Date: 04. September 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 05090/13