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Batch recall of surgical sutures Seralon, Seraflex, Supramid and Terylene, Serag-Wiessner PDF, 129KB, File does not meet accessibility standards Date: 28. October 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 06147/13

Safety notice on angled air hose adapter GA508R used for air motor, Aesculap AG PDF, 101KB, File does not meet accessibility standards Date: 28. October 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04485/13

Field Safety Notice concerning corrective action of software CARINAsim and CARINAiso for laser systems DORADO, LAP GmbH Laser Applikationen PDF, 102KB, File does not meet accessibility standards Date: 24. October 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - others
Reference 06026/13

Urgent Safety Notice for the multifitrate acute renal replacement therapy system with software version 5.2, Fresenius Medical Care GmbH PDF, 126KB, File does not meet accessibility standards Date: 24. October 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 05272/13

Recall of Trial Insertation Instrument ME020R, Aesulap AG PDF, 95KB, File does not meet accessibility standards Date: 21. October 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05838/13

Urgent Field Safety Notice concerning recall of Xomed instrument trays, Medtronic GmbH PDF, 2MB, File does not meet accessibility standards Date: 21. October 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04574/13

Potential safety issue of ViewPoint 6, GE Healthcare PDF, 60KB, File does not meet accessibility standards Date: 21. October 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05737/13

Field Safety Notice concerning AVEA ventilators, CareFusion PDF, 74KB, File does not meet accessibility standards Date: 21. October 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05431/13

Corrective action for NephroCheck Liquid Control, Astute Medical PDF, 154KB, File does not meet accessibility standards Date: 21. October 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 05563/13

Recall of EMBOL-X Glide Protection Systems, Edwards Lifesciences PDF, 81KB, File does not meet accessibility standards Date: 21. October 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05665/13

Lot recall of SelfCat set "Travel", Medical Service GmbH PDF, 37KB, File does not meet accessibility standards Date: 25. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04513/13

Corrective action for Synchron Systems LX20 and UniCel DxC Systems (GLU Reagent), Beckman Coulter PDF, 158KB, File does not meet accessibility standards Date: 24. September 2013 Type: Customer information

Product group In-vitro diagnostics
Reference 03076/10

Safety Notice for the MedStream® programmable Infusion Pumps, Johnson & Johnson Codman PDF, 108KB, File does not meet accessibility standards Date: 24. September 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 04954/13

Important Safety Notice for Stereotactic Circular Collimators, Elekta PDF, 243KB, File does not meet accessibility standards Date: 24. September 2013 Type: Customer information

Product group Radiological technology
Reference 04247/13

Corrective action from Siemens for Immulite® und Immulite® 1000 PSA Third Generation, Siemens PDF, 36KB, File does not meet accessibility standards Date: 24. September 2013 Type: Customer information

Product group In-vitro diagnostics
Reference 04801/13

Corrective action for Hemocue® Urine Albumin Microcuvettes, Hemocue PDF, 151KB, File does not meet accessibility standards Date: 24. September 2013 Type: Customer information

Product group In-vitro diagnostics
Reference 04423/13

Corrective action for Fluoprep, bioMérieux PDF, 52KB, File does not meet accessibility standards Date: 24. September 2013 Type: Customer information

Product group In-vitro diagnostics
Reference 04585/13

Safety Notice for ThermoCool SmartTouch Catheter, Biosense Webster PDF, 2MB, File does not meet accessibility standards Date: 24. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 05278/13

Safety Notice concerning the Leica Ceiling Mounts MSF-1, MS-1F and MC-1F, Leica Microsystems PDF, 166KB, File does not meet accessibility standards Date: 23. September 2013 Type: Customer information

Product group Optics / Precision engineering
Reference 05315/13

Urgent Safety Notice for the Receptal Liners and Canisters, Hospira PDF, 705KB, File does not meet accessibility standards Date: 23. September 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 05351/13

Urgent Safety Notice for highly polished implants, that were packaged in a LDPE bag, Zimmer
PDF, 205KB, File does not meet accessibility standards
Date: 23. September 2013 Type: Customer information

Product group Non-active implants
Reference 05280/13

Lot Recall for the product Intermed Desinfektionsschaum, ISG Intermed Service GmbH & Co. KG PDF, 854KB, File does not meet accessibility standards Date: 20. September 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 05012/13

Corrective action for Hb 201 microcuvettes, Hemocue PDF, 166KB, File does not meet accessibility standards Date: 20. September 2013 Type: Customer information

Product group In-vitro diagnostics
Reference 04606/13

Urgent Safety Notice for the electrically heated Getinge 46 Series Washer Disinfector with PACS 300, Getinge Group PDF, 3MB, File does not meet accessibility standards Date: 20. September 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 04933/13

Urgent Safety Notice for the CardioQ-ODM/CardioQ-ODM+ Monitoring System and accessories, Deltex Medical PDF, 44KB, File does not meet accessibility standards Date: 20. September 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 04712/13

Recall for the Incise Drape, Mölnlycke PDF, 31KB, File does not meet accessibility standards Date: 20. September 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03364/13

Recall for the devices HYAcorp H 1000, HYAcorp H-S 500 and HYAcorp L, BioScience PDF, 763KB, File does not meet accessibility standards Date: 19. September 2013 Type: Customer information

Product group Non-active implants
Reference 04808/13

Urgent Safety Notice for the products Discovery MR450, Discovery MR750, and Optima MR450w, GE Healthcare PDF, 473KB, File does not meet accessibility standards Date: 19. September 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 05324/13

Safety Notice for the EasyUpgrade DR X-ray system, Philips Healthcare PDF, 56KB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Radiological technology
Reference 05291/13