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14,972 results

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Recall of Lipase Reagent, Randox Technical Services / Randox Laboratories Ltd. PDF, 73KB, File does not meet accessibility standards Date: 14. September 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06526/16

Urgent field safety notice for Dimension Vista Enzyme 2 Calibrator / Dimension Enzyme II Calibrator, Siemens Healthcare Diagnostics Inc. PDF, 52KB, File does not meet accessibility standards Date: 14. September 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04386/16

Urgent field safey notice for Vibe Insulin Pump, Animas UK & Ireland / Johnson & Johnson Medical Limited PDF, 274KB, File does not meet accessibility standards Date: 14. September 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 07675/16

Urgent field safety notice for RAPIDPoint 400 / 405 / 500 and RAPIDLab 1200 systems, Siemens Healthcare Diagnostics Inc. PDF, 28KB, File does not meet accessibility standards Date: 14. September 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07335/16

Urgent field safety notice for Syva EMIT II plus opiate assay / Dimension clinical chemistry system and Dimension Vista system / ADVIA chemistry systems, Siemens Healthcare Diagnostics Inc. PDF, 49KB, File does not meet accessibility standards Date: 14. September 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07527/16

Urgent field safety notice for Idylla KRAS Mutation Test, Biocartis NV PDF, 362KB, File does not meet accessibility standards Date: 14. September 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07572/16

Recall of defibrillation electrode Skintact DF29N, Leonhard Lang GmbH PDF, 270KB, File does not meet accessibility standards Date: 14. September 2016 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07722/16

Lot recall of Klerpack BD Syringe Multi-Pack, Life Sciences / Ecolab Ltd. PDF, 113KB, File does not meet accessibility standards Date: 13. September 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 07681/16

Urgent field safety notice for PLATINIUM devices, Sorin Group Deutschland GmbH / LivaNova PLC PDF, 98KB, File does not meet accessibility standards Date: 13. September 2016 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 06554/16

Urgent field safety notice for Getinge ED‐FLOW AER und ED‐FLOW SD AER, Lancer (Getinge Group) PDF, 254KB, File does not meet accessibility standards Date: 13. September 2016 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 07636/16

Lot recall of Sagittal Blade 18.0X.97X90MM, Stryker PDF, 214KB, File does not meet accessibility standards Date: 13. September 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 07800/16

Recall of Accessory Adapter 600525A0, MAQUET GmbH PDF, 286KB, File does not meet accessibility standards Date: 12. September 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07782/16

Lot recall of Concept HeatWave Electrode CS-023, ConMed Corporation PDF, 84KB, File does not meet accessibility standards Date: 12. September 2016 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07344/16

Lot recall of Vanguard 360 Revision Knee System - Tibial Augment Bolts, Zimmer Biomet PDF, 161KB, File does not meet accessibility standards Date: 12. September 2016 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07279/16

Lot recall of TS100S Tubeset Standard Diego Elite, Olympus PDF, 25KB, File does not meet accessibility standards Date: 12. September 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07724/16

Lot recall of EZIO Manual Driver, Teleflex Medical PDF, 95KB, File does not meet accessibility standards Date: 12. September 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07704/16

Lot recall of heart catheter set Oberhavel, hamamed Klinik- und Spezialprodukte GmbH PDF, 63KB, File does not meet accessibility standards Date: 07. September 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 04199/16

Urgent field safety notice for overhead lift Altair / Roomer S, Human Care HC AB PDF, 483KB, File does not meet accessibility standards Date: 07. September 2016 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 07389/16

Lot recall for Straight Ventricular Catheter F8, 25 cm / Integral Lumbar Drainage-Set / CUSA® Dissectron® Fingertip Laparoscopic Cannula, Integra LifeSciences PDF, 278KB, File does not meet accessibility standards Date: 06. September 2016 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 07305/16

Urgent field safety notice for MAGiC (MAGnetic resonance image Compilation) on Signa Pioneer and systems running
Application software version DV25.1., GE Healthcare
PDF, 472KB, File does not meet accessibility standards
Date: 06. September 2016 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 07626/16

Urgent field safety notice for SIGNA Creator and SIGNA Explorer, GE Healthcare PDF, 77KB, File does not meet accessibility standards Date: 06. September 2016 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 07625/16

Lot recall of Comfort Shield® Barrier Cream Cloths, SAGE PRODUCTS LLC PDF, 222KB, File does not meet accessibility standards Date: 06. September 2016 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 07300/16

Urgent field safety notice for Standard Offset Cup Impactor with POM‐C Handle, Greatbatch Medical PDF, 203KB, File does not meet accessibility standards Date: 02. September 2016 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06890/16

Lot recall of 6534‐08N InterActive Implant Open-Tray Transfer Narrow, Implant Direct Sybron Manufacturing LLC PDF, 249KB, File does not meet accessibility standards Date: 02. September 2016 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 07478/16

Urgent field safety notice for Ceiling Lift Altair, Roomer S and HeliQ, Human Care HC AB PDF, 452KB, File does not meet accessibility standards Date: 02. September 2016 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 06424/16

Urgent field safety notice for VITROS Chemistry Products Slide Assays, Ortho Clinical Diagnostics PDF, 853KB, File does not meet accessibility standards Date: 02. September 2016 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07112/16

Batch recall of Nova T 200 copper IUD (intrauterine device), Bayer Pharm AG PDF, 11KB, File does not meet accessibility standards Date: 01. September 2016 Topics: Medical devices Type: Customer information

Product group Contraception - intrauterine device
Reference 09717/15

Lot recall of VIA 27 Microcatheter, Sequent Medical GmbH PDF, 107KB, File does not meet accessibility standards Date: 01. September 2016 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07483/16

Batch recall of TANDEM Bipolar Hip System, Smith & Nephew Inc. PDF, 105KB, File does not meet accessibility standards Date: 01. September 2016 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07441/16

Lot recall of specific EndoWrist® Stapler 45 and 30 instruments for the da Vinci® Xi Surgical System, Intuitive Surgical, Inc. PDF, 613KB, File does not meet accessibility standards Date: 31. August 2016 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 06695/16