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Recall of one manufacturing lot of Procedure Pak called Ophthalmologie - Set I, Mölnlycke Health Care PDF, 16KB, File does not meet accessibility standards Date: 07. October 2010 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 03572/10

Recall of customer specific OP sets, Paul Hartmann AG PDF, 324KB, File does not meet accessibility standards Date: 07. October 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03600/10

Safety Notice for Bilirubin Total (AXON00115), Bilirubin Total (A11A01639) and Bilirubin Jendrassik-Gróf FS (1 0849), AXON Lab PDF, 806KB, File does not meet accessibility standards Date: 07. October 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03521/10

Lot recall of specific lots of NexGen Complete Knee Solution Legacy Knee-Posterior Stabilized LPS Components, Zimmer Inc. PDF, 7MB, File does not meet accessibility standards Date: 07. October 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03458/10

Recall of IntrepideTM coronary stent system, ClearStream PDF, 696KB, File does not meet accessibility standards Date: 30. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02980/10

Field Safety Notice concerning Hologic StereoGuide Biopsy System, Medicor PDF, 914KB, File does not meet accessibility standards Date: 30. September 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02936/10

Field Safety Notice concerning BeneHeart D6 defibrillator / monitor, Shenzhen Mindray Bio-Medical Electronics Co., Ltd. PDF, 1MB, File does not meet accessibility standards Date: 30. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03470/10

Safety Information concerning LIAISON® VZV IgG and LIAISON® VZV IgM, DiaSorin S.p.A PDF, 959KB, File does not meet accessibility standards Date: 30. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02477/10

Field Safety Notice concerning a problem with the TxT table for Siemens Linear Accelerator Oncor Impession Plus, Siemens Healthcare PDF, 84KB, File does not meet accessibility standards Date: 29. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04510/09

Recall for Whole Blood Controls RQCHRT for Use with Hemochron Kaolin and Celite HRT Test Tubes (Lot no. H9KHR002 and B0KHR001), ITC PDF, 28KB, File does not meet accessibility standards Date: 29. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02475/10

Lot recall of OXOID IDEIA Lyme Neuroborreliosis, OXOID Ltd./Thermo Fisher Scientific PDF, 2MB, File does not meet accessibility standards Date: 28. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03296/10

Safety Notice for OEC 9800 X-ray systems, GE Healthcare PDF, 726KB, File does not meet accessibility standards Date: 28. September 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03227/06

Lot recall of Arthroscopy Outflow/Suction Tubing Sets, ConMed Linvatec Corporation PDF, 3MB, File does not meet accessibility standards Date: 28. September 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03406/10

Recall of Roche Molecular Systems for Tina-quant D-Dimer Gen. 2, Roche Diagnostics PDF, 72KB, File does not meet accessibility standards Date: 28. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02849/10

Safety Notice for DYONICS BONECUTTER ELECTROBLADE, Smith & Nephew PDF, 708KB, File does not meet accessibility standards Date: 28. September 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02924/10

Recall for Sterimedix/Altomed Ophthalmic Irrigation/Aspiration Coaxial Handpieces/Bimanual Handles, Sterimedix Ltd. PDF, 374KB, File does not meet accessibility standards Date: 27. September 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02460/10

Corrective Action for ARCHITECT iVancomycin Reagent, Abbott PDF, 133KB, File does not meet accessibility standards Date: 27. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03361/10

Recall for ARCHITECT Tacrolimus Reagent, Abbott PDF, 28KB, File does not meet accessibility standards Date: 27. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03360/10

Safety Notice for SynchroMed II, Medtronic PDF, 43KB, File does not meet accessibility standards Date: 27. September 2010 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03411/10

Recall for Sonopet Ultrasonic Aspirator Console, Stryker PDF, 548KB, File does not meet accessibility standards Date: 27. September 2010 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02997/10

Recall for Octopus Nuvo Tissue Stabilizer, Medtronic PDF, 42KB, File does not meet accessibility standards Date: 27. September 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03430/10

Safety Notice for Ultimate Endo Retrieval Pouch, Cory Bros PDF, 128KB, File does not meet accessibility standards Date: 27. September 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02527/10

Recall for C5L PLATELET SET (5-DAY STORAGE), Fresenius PDF, 75KB, File is accessible Date: 24. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03384/10

Safety Notice for Medtronic CoreValve® Delivery system, Medtronic PDF, 14KB, File does not meet accessibility standards Date: 24. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03204/10

Corrective action for Synchron Systems LX20 and UniCel DxC Systems only GLU Reagent, Beckman Coulter PDF, 110KB, File does not meet accessibility standards Date: 24. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03076/10

Safety Notice for EVO Clinical 100-Analyser, Tecan PDF, 38KB, File does not meet accessibility standards Date: 24. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01826/10

Safety Notice related to the Synthes SynFix-LR Technique Guide, Synthes PDF, 91KB, File does not meet accessibility standards Date: 24. September 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03072/10

Recall for Encore® Microptic® surgical gloves, Ansell PDF, 44KB, File does not meet accessibility standards Date: 23. September 2010 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03253/10