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Field Safety Notice concerning a corrective action of Corpuls 3 defibrillators to which software versions 2.0.0 and 2.0.2 have been installed, GS Elektromedizinische Geräte G. Stemple GmbH PDF, 503KB, File does not meet accessibility standards Date: 17. December 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07316/12

Lot Recall for Perthese & Perthese Esthea Breast Implants, Perouse Plastie PDF, 92KB, File does not meet accessibility standards Date: 12. December 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 07319/12

Recall for several RUMI ARCH® and Advincula Arch™ uterine manipulation handles, Cooper Surgical PDF, 56KB, File does not meet accessibility standards Date: 12. December 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07453/12

Recall for Wang Transbronchial Aspiration Needles, ConMed Corporation PDF, 56KB, File does not meet accessibility standards Date: 12. December 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07367/12

Recall flexible drills, tantum PDF, 37KB, File does not meet accessibility standards Date: 07. December 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07007/12

Refitting of wheelchairs LifeStand LSCO, Permobil PDF, 135KB, File does not meet accessibility standards Date: 07. December 2012 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 07303/12

Field Safety Notice concerning potentially falsely placed electronic left/right markers on DigitalDiagnost X-ray systems, Philips Medical Systems PDF, 94KB, File does not meet accessibility standards Date: 06. December 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07296/12

Field Safety Notice concerning dosing problem of EndoDis in ETD2 with PAA upgrade kit, Olympus PDF, 31KB, File does not meet accessibility standards Date: 06. December 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 06295/12

Field Safety Notice concerning safety issue because of an unintended rotation of the Gantry of Linear Accelerators Primus / Oncor / Artiste, Siemens Healthcare PDF, 86KB, File does not meet accessibility standards Date: 06. December 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 04247/12

Software Upgrade required on DigitalDiagnost X-ray systems with software versions 2.0.2 und 2.1.3, Philips Medical Systems PDF, 103KB, File does not meet accessibility standards Date: 29. November 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07281/12

Complementary information on the Recall of the Hyperion Extension Sleeves 25 mm and 30 mm, Biomet PDF, 58KB, File does not meet accessibility standards Date: 29. November 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06732/12

Recall of the MobiCath Bi-Directional Guiding Sheaths with large and small curve, Greatbatch Medical Ltd. PDF, 264KB, File does not meet accessibility standards Date: 29. November 2012 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 07097/12

Recall of several Attachments and Cutting Burrs, The Anspach Effort Inc. PDF, 221KB, File does not meet accessibility standards Date: 28. November 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 06985/12

Recall for BRAHMS Free βhCG KRYPTOR in combination with BRAHMS Free βhCG KRYPTOR CAL, ThermoFisher PDF, 1MB, File does not meet accessibility standards Date: 28. November 2012 Type: Customer information

Product group In-vitro diagnostics
Reference 06874/12

Recall for the Trochanteric Fixation Nailing System (TFN), Synthes GmbH PDF, 115KB, File does not meet accessibility standards Date: 28. November 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06962/12

Recall for BRAHMS Osteocalcin KRYPTOR, ThermoFisher PDF, 701KB, File does not meet accessibility standards Date: 28. November 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06638/12

Recall for the Zimmer Persona™ Tibial Drill, Tibial Implants, and Various Instruments, Zimmer Inc. PDF, 54KB, File does not meet accessibility standards Date: 27. November 2012 Type: Customer information

Product group Medical instruments for use in humans
Reference 07220/12

Corrective action for ADAMS A1c HA-8160, ARKRAY Date: 27. November 2012 Type: Customer information

Product group In-vitro diagnostics
Reference 06564/12

Recall for Troponin I Schnelltest, DiaSys Greiner PDF, 67KB, File does not meet accessibility standards Date: 26. November 2012 Type: Customer information

Product group In-vitro diagnostics
Reference 05671/12

Recall for Oxoid Antimicrobial Susceptibility Testing Disc F100, ThermoFisher PDF, 164KB, File does not meet accessibility standards Date: 26. November 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06904/12

Corrective Action for ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CP, Siemens PDF, 121KB, File does not meet accessibility standards Date: 26. November 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07082/12

Recall of several sterilization indicators (STERRAD CycleSure 24 Biological Indicator) and sets, ASP PDF, 271KB, File does not meet accessibility standards Date: 20. November 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 06971/12

Safety Notice for Artis zeego systems with SW revision VC14, VC20 and VC21, Siemens Healthcare PDF, 37KB, File does not meet accessibility standards Date: 20. November 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 06855/12

Safety Notice concerning corrective actions of cardioLife defibrillators series TEC-5521K and TEC-5531K, Nihon Kohden Europe GmbH PDF, 41KB, File does not meet accessibility standards Date: 20. November 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06805/12

Safety Notice for the Mobilett Mira, Siemens Healthcare PDF, 1MB, File does not meet accessibility standards Date: 19. November 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - mobile radiological diagnostic facilities
Reference 05851/12

Safety Notice for Artis Zee / Zeego systems, Siemens Healthcare PDF, 37KB, File does not meet accessibility standards Date: 19. November 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 05323/12

Updated Safety Notice / Recall for the ABGII Modular Systems, Stryker PDF, 33KB, File does not meet accessibility standards Date: 19. November 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03016/12

Safety Notice for the product MOSAIQ, Elekta PDF, 263KB, File does not meet accessibility standards Date: 15. November 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 06109/12