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Recall for Pediatric/Neonatal Wire Attached ECG Electrodes, ConMed PDF, 149KB, File does not meet accessibility standards Date: 21. October 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03503/10

Recall for C5L PLATELET SET (5-DAY-STORAGE), Fresenius Kabi PDF, 140KB, File does not meet accessibility standards Date: 20. October 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03673/10

Rückruf bestimmer Los-Nummern des Produktes Rotacrush, Medwork Medical products and services GmbH PDF, 206KB, File does not meet accessibility standards Date: 08. October 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03507/10

Lot recall of device Rotacrush, Medwork Medical products and services GmbH PDF, 206KB, File does not meet accessibility standards Date: 08. October 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03507/10

Safety information regarding malfunction of Novalung Vision alpha, Novalung GmbH PDF, 299KB, File does not meet accessibility standards Date: 08. October 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03450/10

Safety information to pay attention to correct use of medical apparatus G-scan, Esaote Biomedica GmbH PDF, 13KB, File does not meet accessibility standards Date: 08. October 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01120/10

Recall of Babix holder at VS wallstands of BuckyDiagnost, EasyDiagnost and DigitalDiagnost X-ray systems, Philips PDF, 26KB, File does not meet accessibility standards Date: 08. October 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01107/10

Exchange of siderail screws in hospital beds Eleganza 3 and Eleganza 3XC, Linet PDF, 89KB, File does not meet accessibility standards Date: 08. October 2010 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03212/10

Lot recall for IMMULITE 2500 HCG (L5KCG2,6), Siemens PDF, 31KB, File does not meet accessibility standards Date: 08. October 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03559/10

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