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Lot Recall for the XIA 3 Titanium ILIAC Screwdrivers, Stryker Spine PDF, 12KB, File does not meet accessibility standards Date: 09. January 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07995/12

Safety Notice for the Aliquot Bone Cement Delivery System, Stryker PDF, 423KB, File does not meet accessibility standards Date: 09. January 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07287/12

Recall for the Linx Reflux Management System Esophagus Sizing Tool LSS-2, Torax Medical Inc. PDF, 84KB, File does not meet accessibility standards Date: 09. January 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 07364/12

Urgent Field Safety Notice for the Cadisc™-C Endplate Handles and Blades, Ranier Technology Limited PDF, 1MB, File does not meet accessibility standards Date: 08. January 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07151/12

Lot Recall for 6,5mm cancellous bone screws 25mm and 35mm, Stryker PDF, 5MB, File does not meet accessibility standards Date: 08. January 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 05711/12

Safety Notice for Alaris® GP Infusion System, CareFusion Switzerland PDF, 49KB, File does not meet accessibility standards Date: 08. January 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 07078/12

Safety Notice concerning the depth gauge 80-0623, Acumed LLC. PDF, 177KB, File does not meet accessibility standards Date: 08. January 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07615/12

Safety Notice for Philips IntelliVue Information Center (PIIC) and Philips IntelliVue Information Center iX (PIIC iX), Philips Healthcare PDF, 121KB, File does not meet accessibility standards Date: 07. January 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07444/12

Safety Notice for Infinity® Acute Care System (IACS) with DualHemo Mcable, Dräger Medical GmbH PDF, 100KB, File does not meet accessibility standards Date: 07. January 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07419/12

Urgent Safety Notice for Patient Data Module (PDM) Version 2.0,GE Healthcare PDF, 69KB, File does not meet accessibility standards Date: 07. January 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07981/12

Lot Recall for the Alaris® IVAC® 590 Series Blood Set, CareFusion PDF, 56KB, File does not meet accessibility standards Date: 07. January 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01960/12

Lot Recall for the Penumbra System Canisters (PAPS1), Penumbra PDF, 3MB, File does not meet accessibility standards Date: 07. January 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04543/12

Safety Notice for the products NeuViz Dual and NeuViz 16, Neusoft Medical Systems PDF, 3MB, File does not meet accessibility standards Date: 04. January 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 06944/12

Lot Recall for the UNIEVER Epidural/Combined Spinal Epidural Anesthesia Minitray, UNISIS Corp. PDF, 312KB, File does not meet accessibility standards Date: 04. January 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - injection kits
Reference 07295/12

Safety Notice regarding Neria steel cannula infusion sets, ConvaTec PDF, 59KB, File does not meet accessibility standards Date: 04. January 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 05245/12

Safety Notice on pacemakers (Models Accent SR PM1110 and Accent DR PM2112), St. Jude Medical PDF, 235KB, File does not meet accessibility standards Date: 04. January 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - cardiac pacemakers
Reference 07477/12

Safety Notice concerning a potential DRX-1 Console wiring error, Carestream Health PDF, 20KB, File does not meet accessibility standards Date: 04. January 2013 Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07174/12

Corrective Action for the TCM4 series Base Unit, Radiometer PDF, 32KB, File does not meet accessibility standards Date: 03. January 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07327/12

Safety Information for the Versys® and Slotted Provisional Femoral Heads, Zimmer Inc. PDF, 78KB, File does not meet accessibility standards Date: 03. January 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07261/12

Lot Recall of STERRAD® NX® System Cassettes REF 10133, ASP PDF, 44KB, File does not meet accessibility standards Date: 03. January 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 07558/12

Lot Recall of the Coaxial Interventional Needles, Innovative Tomography Products GmbH PDF, 444KB, File does not meet accessibility standards Date: 28. December 2012 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 07673/12

Lot Recall of the Alphacard single-use syringe for intra-atrial ECG lead, B. Braun Melsungen AG PDF, 295KB, File does not meet accessibility standards Date: 28. December 2012 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 07701/12

Recall of the ENSEAL® G2 Curved and Straight Tissue Sealer devices, Ethicon Endo-Surgery PDF, 33KB, File does not meet accessibility standards Date: 28. December 2012 Type: Customer information

Product group Electromedical fields
Reference 07325/12

Recall for Antimicrobial Susceptibility Testing Disc, Oxoid PDF, 17KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07555/12

Lot Recall of TRIGEN INTERTAN nails, SMITH & NEPHEW PDF, 97KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07646/12

Safety Notice concerning the Metran High Frequency Oscillation Ventilator model R100/Vision a, Novalung PDF, 453KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07357/12

Safety Notice concerning LIVOPAN systems, Linde Gas Therapeutics PDF, 98KB, File does not meet accessibility standards Date: 27. December 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07611/12

Recall of the ARDIS Inserter worldwide, Zimmer Inc. PDF, 131KB, File does not meet accessibility standards Date: 27. December 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07561/12

Recall of GlideScope GVL video laryngoscope, Verathon PDF, 2MB, File does not meet accessibility standards Date: 20. December 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 06957/12

Corrective Action concerning Oxoid Columbia Agar with Sheep Blood PLUS PB 5039 A (Lot- No: 1262841) due to a microbial contamination, OXOID PDF, 108KB, File does not meet accessibility standards Date: 17. December 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07105/12