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Lot recall of custom specific procedure trays containing Urine Drainage Bags by Unomedical A/S, ArcRoyal Ltd. PDF, 116KB, File does not meet accessibility standards Date: 24. February 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00135/11

Field Safety Notice regarding „ Power Station, type number 0101-24937 and 0701-24906”, ResMed PDF, 448KB, File does not meet accessibility standards Date: 24. February 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03086/10

Recall of double foot switch KF21, Ziehm PDF, 534KB, File does not meet accessibility standards Date: 22. February 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00533/11

Safety Notice concerning user instructions for laser device Dornier Medilas D UroBeam, Dornier MedTech Laser GmbH PDF, 698KB, File does not meet accessibility standards Date: 22. February 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 00315/10

Safety Information on potential risk regarding device „Cholestech LDX ® Lipid Profile GLU Test Cassettes“, Alere San Diego PDF, 792KB, File does not meet accessibility standards Date: 22. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00766/11

Lot recall of one Hydrofilm variant, Paul Hartmann AG PDF, 87KB, File does not meet accessibility standards Date: 21. February 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 00673/11

Three new warning statements in Instruction for Use for VCARE® Vaginal-Cervical Ahluwalia’s Retractor-Elevator, ConMed Corporation PDF, 543KB, File does not meet accessibility standards Date: 21. February 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00672/11

Safety issue with Operating Table TITAN, Trumpf Medizin Systeme GmbH PDF, 2MB, File does not meet accessibility standards Date: 21. February 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00166/11

Safety Information concerning VSX10030HD Videoscope, VIMS PDF, 2MB, File does not meet accessibility standards Date: 18. February 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02393/09

Recall of HLA Fusion Version 2.0.0-SP1, One Lambda PDF, 402KB, File does not meet accessibility standards Date: 18. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00291/11

Lot recall of Inhibin A ELISA Kits (Ref.: DSL-10-28100-4, DSL-10-28100T-4), Beckman Coulter PDF, 620KB, File does not meet accessibility standards Date: 17. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00115/11

Safety Notice concerning additional safety precautions for Horizon Cardiology Hemo monitoring system, McKesson PDF, 404KB, File does not meet accessibility standards Date: 17. February 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04850/10

Lot-dependent recall of PRISM Reaction Trays, Abbott PDF, 82KB, File does not meet accessibility standards Date: 17. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04823/10

Safety Notice regarding device TomoTherapy® Treatment System, ThomoTherapy Incorporated PDF, 639KB, File does not meet accessibility standards Date: 16. February 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00443/11

Corrective action for TruCal Apo A1 (Lot-No. 13785 – 13787), DiaSys PDF, 2MB, File does not meet accessibility standards Date: 16. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00424/11

Safety Notice on Ankylos Implant driver C/X with screwdriver, FRIADENT GmbH PDF, 1MB, File does not meet accessibility standards Date: 16. February 2011 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 04672/10

Safety Notice for ApexPro Telemetry System, GE Healthcare PDF, 433KB, File does not meet accessibility standards Date: 10. February 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00477/11

Safety Notice concerning a corrective action of the BeneHeart D6 defibrillator/monitor, Shenzhen Mindray Bio-Medical Electronics Co., Ltd. PDF, 287KB, File does not meet accessibility standards Date: 04. February 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00318/11

Safety Notice for AK 200 ULTRA S and AK 200 ULTRA (Incorrect online priming), Gambro PDF, 61KB, File does not meet accessibility standards Date: 04. February 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04754/10

Safety Notice concerning refilling of implantable drug pumps, Medtronic PDF, 41KB, File does not meet accessibility standards Date: 04. February 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00076/11

Recall for STA Neoplastin R, Diagnostica Stago / Roche Diagnostics PDF, 23KB, File does not meet accessibility standards Date: 04. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04828/10

Lot Recall for SynCage-C spine implants, SYNTHES PDF, 59KB, File does not meet accessibility standards Date: 04. February 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04833/10

Urgent Safety Notice for CADD®-Solis Pumps, Smiths Medical PDF, 125KB, File does not meet accessibility standards Date: 03. February 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00380/11

Safety Notice on some wrongly mounted locks, Andreas Hettich GmbH & Co. KG PDF, 64KB, File does not meet accessibility standards Date: 03. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03683/10

Recall for Slidex Staph Kit, Biomerieux PDF, 62KB, File does not meet accessibility standards Date: 03. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04816/10

Safety Notice for Olympus Pediatric Resection Electrodes, Olympus Winter & Ibe GmbH PDF, 36KB, File does not meet accessibility standards Date: 03. February 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04690/10

Lot Recall for procedure trays containing Urine Drainage Bags by Unomedical A/S, Paul Hartmann AG PDF, 93KB, File does not meet accessibility standards Date: 02. February 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00143/11

Safety Notice for Bilirubin Auto Total FS, DiaSys Diagnostics Systems PDF, 208KB, File does not meet accessibility standards Date: 02. February 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03184/10