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14,984 results

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Safety Notice for implantable pulse generators for neurostimulation Eon, Eon Mini and Brio, St. Jude Medical PDF, 37KB, File does not meet accessibility standards Date: 24. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 05919/11

Safety Notice for Hamilton-G5 and Hamilton-S1 ventilators, Hamilton Medical PDF, 387KB, File does not meet accessibility standards Date: 24. February 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00841/12

Recall of mobile pneumatic drivers Freedom Driver System, Syncardia Systems Inc. PDF, 41KB, File does not meet accessibility standards Date: 24. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 05879/11

Recall of Companion 2 Drivers, Syncardia Systems PDF, 45KB, File does not meet accessibility standards Date: 23. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 06025/11

Recall of controller units of implantable HeartWare VAS, HeartWare Inc. PDF, 1MB, File does not meet accessibility standards Date: 23. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 05925/11

Recall of implantable pulse generators for neurostimulation Eon Mini and Brio, St. Jude Medical PDF, 39KB, File does not meet accessibility standards Date: 23. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 05924/11

Recall of implantable left ventricular assist device systems HeartAssist 5 LVAS, MicroMed Cardiovascular Inc. PDF, 636KB, File does not meet accessibility standards Date: 22. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 03533/11

Safety Information for the implantable left ventricular assist devices Incor, BerlinHeart PDF, 41KB, File does not meet accessibility standards Date: 22. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 04841/10

Recall of Software and Urgent Field Safety Notice according to HeartAssist 5 LVAS, MicroMed Cardiovascular Inc. PDF, 465KB, File does not meet accessibility standards Date: 22. February 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 00980/11

Safety Notice for Gliding Nail Blade Handle, SMITH&NEPHEW PDF, 82KB, File does not meet accessibility standards Date: 22. February 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00451/12

Software-Update of the treadmills of the PPS Series, Woodway GmbH PDF, 211KB, File does not meet accessibility standards Date: 21. February 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - functional diagnostics by way of gas exchange and exercise
Reference 00158/11

Corrective Action of specific Trilogy Ventilators, Philips Respironics PDF, 24KB, File does not meet accessibility standards Date: 21. February 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00460/12

Lot Recall for the Hedstroem root canal file, HAGER & MEISINGER PDF, 88KB, File does not meet accessibility standards Date: 21. February 2012 Topics: Medical devices Type: Customer information

Product group Dental products - instruments
Reference 00012/12

Incorrect position readout values caused by excessive connector resistance of C-Series Clinac® Models, Varian medical systems PDF, 206KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 00805/12

Lot recall of cardiac guide wire, OptiMed Medizinische Instrumente GmbH PDF, 650KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00776/12

Recall of all articles of cyclOS Putty, MATHYS European Orthopaedics PDF, 198KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00774/12

Recall of Masstrak Immunosuppressants XE RUO Kit, Waters PDF, 103KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00743/12

Recall of all unexpired lots of „S.M.A.R.T. CONTROL“ Nitinol Stent System, Cordis PDF, 162KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00629/12

Field safety notice for VariSeed users, Varian Medical systems PDF, 178KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
Reference 00530/12

Corrective Action for IMMULITE CK-MB, Siemens PDF, 71KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00504/12

Recall of ATB ANA EU Kit, BioMerieux PDF, 234KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00452/12

Recall of Active Renin IRMA Test Kit, Beckman Coulter PDF, 29KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00420/12

Corrective Action for clinical Chemistry Analyzers AU2700 / AU2700 Plus and AU5400, Beckman Coulter PDF, 135KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00389/12

Corrective Action for primary antibodies to CD2 and CD7, Leica Biosystems PDF, 299KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00364/12

Corrective Action for Dimension Vista Systems Software Version 3.4, Siemens PDF, 31KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06034/11

Failure in XVI, Elekta PDF, 237KB, File does not meet accessibility standards Date: 16. February 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 00356/12

Batch recall of SUSI Instruments because of potential insterility, Aesculap AG PDF, 168KB, File does not meet accessibility standards Date: 16. February 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 00807/12

Safety issue with 4D Planning procedure option of MultiPlan® Treatment Planning System, Accuray PDF, 318KB, File does not meet accessibility standards Date: 15. February 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00673/12

Error in software catalog number 71070401 for external fixator Spatial Frame, Smith & Nephew Orthopaedics GmbH PDF, 82KB, File does not meet accessibility standards Date: 15. February 2012 Topics: Medical devices Type: Customer information

Product group Medical data processing (software) - others
Reference 00580/12

Software update for Leica M822 F20 and M822 F40 surgical microscopes required, Leica Microsystems PDF, 111KB, File does not meet accessibility standards Date: 15. February 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 00400/12