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Software error in the Schwind CAM software from Schwind eye-tech-solutions PDF, 86KB, File does not meet accessibility standards Date: 02. February 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03687/06

Safety information for the wheelchair model 1.300 UF from Uniroll PDF, 118KB, File does not meet accessibility standards Date: 02. February 2007 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03781/06

Corrective action of the cards for susceptibility testing for the analyzers Vitek, Vitek 2 and Vitek compact from bioMèrieux PDF, 96KB, File does not meet accessibility standards Date: 02. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00339/07

Corrective action of the Vitek GPS-531, Vitek GPS-532 and Vitek GPS-533 cards for susceptibility testing from bioMèrieux PDF, 55KB, File does not meet accessibility standards Date: 02. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00318/07

Corrective action and recall of the Sample Management System (software version 2.2) from DPC Biermann PDF, 84KB, File does not meet accessibility standards Date: 01. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00261/07

Software update for the Telemetrie-Systems ApexPro/ApexPro CH from GE Healthcare PDF, 73KB, File does not meet accessibility standards Date: 01. February 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03795/06

Recall of ConMed Linvatec Ultra Power Burs and ConMed Linvatec E9000 Burs PDF, 776KB, File does not meet accessibility standards Date: 01. February 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03746/06

Recall of the Syva Emit 2000 Phenobarbital test from Dade Behring PDF, 39KB, File does not meet accessibility standards Date: 30. January 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00194/07

Corrective action concerning the Integris and Allura Xper X‑Ray Systems from Philips PDF, 70KB, File does not meet accessibility standards Date: 30. January 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00269/07

Corrective action of the clinical chemistry system Dimension RxL Max with STM from Dade Behring PDF, 26KB, File does not meet accessibility standards Date: 30. January 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00193/07

Recall of 20 Gauge Millenium Lightening High-Speed Cutter Tips and vitrectomy packs from Bausch & Lomb PDF, 132KB, File does not meet accessibility standards Date: 29. January 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03709/06

Corrective action for Total Bilirubin OSR of Olympus PDF, 47KB, File does not meet accessibility standards Date: 29. January 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00162/07

Recall of control unit model PowerLink3 from Rehavista PDF, 60KB, File does not meet accessibility standards Date: 29. January 2007 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03854/06

Recall of Bard Composix Kugel Patches Large PDF, 127KB, File does not meet accessibility standards Date: 29. January 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00213/07

Information about Prismaflex Continuous Renal Replacement System from Gambro Lundia AB PDF, 55KB, File does not meet accessibility standards Date: 29. January 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00027/07

Corrective action for Advia Centaur Acid and base reagents of Bayer PDF, 57KB, File does not meet accessibility standards Date: 29. January 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03772/06

Recall of HeartStart FR2+ Automated External Defibrillators, models M3860A, M3861A, M3840A and M3841A from Philips Medizin Systeme Böblingen PDF, 42KB, File does not meet accessibility standards Date: 26. January 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00225/07

Recall and corrective action for FC 500 MPL Flow Cytometry Systems with MXP Software (versions 2.0 and 2.1) from Beckman Coulter PDF, 45KB, File does not meet accessibility standards Date: 25. January 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03232/06

Recall of heated breathing circuits from Fisher & Paykel PDF, 114KB, File does not meet accessibility standards Date: 25. January 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03676/06

Information about the system PRECISION PLUS® (TUNA®) from Medtronic PDF, 175KB, File does not meet accessibility standards Date: 24. January 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03754/06

Recall of sterile markers and kits for surgical navigation from Praxim Medivision PDF, 257KB, File does not meet accessibility standards Date: 24. January 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03822/06

Information about the AQUARIUS Haemofiltration machine from Edwards Lifesciences PDF, 46KB, File does not meet accessibility standards Date: 23. January 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00016/07

Recall of Tracheotomy Tubes from Unomedical PDF, 77KB, File does not meet accessibility standards Date: 23. January 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00141/07

Information about the BD Careflow™ Central Venous Catheter from Becton Dickinson PDF, 548KB, File does not meet accessibility standards Date: 23. January 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00153/07

Recall of Beaver Mini-Blades from Becton Dickinson PDF, 78KB, File does not meet accessibility standards Date: 22. January 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 00079/07

Information for the MODUS® MDO 1.5 Le Fort I distraktor from Medartis PDF, 28KB, File does not meet accessibility standards Date: 18. January 2007 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 00567/06

Information concerning the using of the GM cervical sleeves with the CT/MR Ring & Tandem Applicator Set from Varian PDF, 60KB, File does not meet accessibility standards Date: 17. January 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03663/06

Recall of the Imipenem 10 µg Antimicrobial Susceptibility Discs from Oxoid PDF, 83KB, File does not meet accessibility standards Date: 17. January 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03770/06