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Problems with the Corometrics 17x series fetal monitors from GE Healthcare Technologies PDF, 95KB, Date: 21. November 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02700/05

Nephros recalls the OLpur MD 190 PDF, 34KB, Date: 14. November 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02631/05

Corrective action of Dade Behring for Berichrom AI III (A) Kits OWWR PDF, 91KB, Date: 14. November 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02637/05

Corrective action and recall from Emergo Europe for i-Stat G3+ Cartridges PDF, 39KB, Date: 14. November 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02218/05

Recall of Medtronic Model 9013G0711 and 9013G0712 and FHC Model FC1008-66 Motor Options used with Medtronic microTargeting drives PDF, 73KB, Date: 10. November 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02738/05

Recall of the Vidaurri LASIK Flap Irrigators from Oasis Medical PDF, 101KB, Date: 10. November 2005 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02414/05

Prosan informs on how to proceed if during removal of the IUD type Flexi-T 300 the IUD thread is detached or not visible PDF, 79KB, Date: 10. November 2005 Topics: Medical devices Type: Customer information

Product group Contraception
Reference 00746/05

Change in the Instructions for Use of the ASICO Royal Unihand Injectors PDF, 354KB, Date: 10. November 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00242/05

Stryker recalls further lot numbers of T2 Recon Lag Screw PDF, 179KB, File does not meet accessibility standards Date: 04. November 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01974/05

Recall of the CORE Powered Instument Driver from Stryker PDF, 38KB, Date: 28. October 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02054/05

Disconnection of the internal oxygen hose connexion inside the Datex-Ohmeda S/5 Aespire- anaesthesia machine of GE Healthcare PDF, 85KB, Date: 28. October 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02628/05

Transient suspension for the product for sales and marketing from Tropon PDF, 66KB, Date: 28. October 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02480/05

Correct handling of the Talon™ and Symmetry™ Angioplasty Balloon Dilatation Catheters PDF, 104KB, Date: 28. October 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02629/05

Corrective action of BioMerieux for VeriCal PDF, 109KB, Date: 28. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02444/05

Additional cleaning and disinfection of Hydrotherapy devices from BEKA PDF, 12KB, Date: 27. October 2005 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 01796/05

Recall of intraocular lenses from Advanced Medical Optics PDF, 132KB, Date: 27. October 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02549/05

Advisory Notice from Medtronic for Valiant Thoracic Stent Graft PDF, 56KB, Date: 27. October 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02430/05

Incorrect pictures with the Centricity Carddas IMS AI 1000 workstation from GE Healthcare Technologies PDF, 66KB, Date: 27. October 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02624/05

Recall and corrective action of Beckman Coulter for Synchron LX systems PDF, 62KB, Date: 27. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02457/05

Corrective action for Synchron Systems C Reactive Protein Reagent, Beckman Coulter PDF, 12KB, Date: 27. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01950/05

Corin Medical recalls the Uniglide Femoral Drills PDF, 53KB, Date: 24. October 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02483/05

Aesculap recommends to check the tibia preparation plateaus PDF, 111KB, Date: 24. October 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02467/05

Recall of Dade Behring for Dade Actin FS PDF, 55KB, Date: 24. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02418/05

Recall of Roche for Elecsys Assay Tips PDF, 164KB, Date: 24. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02522/05

Potential failure with the Image Navigator function of the SIENET COSMOS Workplace from Siemens PDF, 48KB, Date: 19. October 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02329/05

eVent Medical recalls the Inspiration Ventilator System PDF, 121KB, Date: 19. October 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02354/05

Single incident during the use of a flexible implant tube with blind end from Varian PDF, 1MB, Date: 19. October 2005 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02453/05

AGA Medical recalls the AMPLATZER® Duct Occluder PDF, 98KB, Date: 18. October 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02295/05

Advice for electronic wheelchair Allround 960 C, Ortopedia PDF, 44KB, Date: 18. October 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01862/03

Recall of DakoCytomation for HercepTest PDF, 114KB, Date: 18. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02525/05