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Corrective action from Roche for Total Bilirubin Granulat PDF, 125KB, File does not meet accessibility standards Date: 18. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02581/08

Corrective action and recall of Roche for Cobas 6000 Analyzers PDF, 928KB, File does not meet accessibility standards Date: 18. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03970/08

Field safety notice to iSite PACS PDF, 39KB, File does not meet accessibility standards Date: 18. November 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02879/08

Field safety notice from BrainLAB PDF, 2MB, File does not meet accessibility standards Date: 18. November 2008 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03029/08

Corrective Action of Siemens Healthcare Diagnostics Inc. for IMMULITE PDF, 98KB, File does not meet accessibility standards Date: 18. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04039/08

Field Safety Notice about a recall of the joysticks from the Axiom Luminos dRF from Siemens Healthcare PDF, 1MB, File does not meet accessibility standards Date: 18. November 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03945/08

Recall of the infusion device Infudrop Air matic PY from Fresenius Kabi AG PDF, 3MB, File does not meet accessibility standards Date: 18. November 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03531/08

Recall from the manufacturer C.R. Bard, lots of 20 F Ponsyk Non Balloon Replacement Gastrostomy Tube PDF, 2MB, File does not meet accessibility standards Date: 17. November 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02775/08

Recall from DiaSys for TruCal HbA1c liquid Product codes PDF, 1,023KB, File does not meet accessibility standards Date: 17. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04173/08

Recall from Respironics of BIPAP Focus ventilators PDF, 1,008KB, File does not meet accessibility standards Date: 17. November 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03792/08

Recall of the Tender Flow Pediatric Arterial Cannulae from Terumo Cardiovascular Systems Corporation PDF, 3MB, File does not meet accessibility standards Date: 17. November 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04073/08

Field Safety Notice from Maquet GmbH & Co. KG on pedals 1009.81 for operating tables PDF, 2MB, File does not meet accessibility standards Date: 17. November 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04060/08

Recall from BioMerieux for Vitek 2 GN identification cards PDF, 632KB, File does not meet accessibility standards Date: 17. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04251/08

Corrective action of Beckman Coulter for UniCel peristaltic pumps PDF, 2MB, File does not meet accessibility standards Date: 17. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04249/08

Corrective action from Roche Diagnostics GmbH for calibration parameters with MODULAR ANALYTICS PDF, 60KB, File does not meet accessibility standards Date: 12. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01059/08

Field Safety Notice from Johnson & Johnson Medical GmbH for implantable infusion pump model Archimedes PDF, 46KB, File does not meet accessibility standards Date: 12. November 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01307/08

Field Corrective Action from R 82 A/S of High-Low X-Frames PDF, 386KB, File does not meet accessibility standards Date: 12. November 2008 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 04076/08

Otto Bock Healthcare GmbH recalls Knee Joints model 3R66 with certain serial numbers. PDF, 86KB, File does not meet accessibility standards Date: 12. November 2008 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 04112/08

Corrective Action of Siemens Healthcare Diagnostics Inc. for Dimension Vista System V-LYTE Integrated Multisensor PDF, 57KB, File does not meet accessibility standards Date: 12. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03901/08

Information from Stryker of Vision Elect 26-Zoll-HDTV Monitors PDF, 207KB, File does not meet accessibility standards Date: 12. November 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03705/08

Recall of Ortho-Clinical Diagnostics for VITROS Chemistry Products Calibrator Kit 2 PDF, 5MB, File does not meet accessibility standards Date: 10. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03837/08

Corrective Action of Diagnostica Stago for reagents PDF, 611KB, File does not meet accessibility standards Date: 10. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03587/08

Corrective action / Recall of Oxoid Germany - Thermo Fisher Scientific for PB5039A PDF, 621KB, File does not meet accessibility standards Date: 10. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03965/08

Corrective action / Recall of Oxoid Germany - Thermo Fisher Scientific PDF, 586KB, File does not meet accessibility standards Date: 10. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03964/08

Field Safety Notice concerning a software update of the defibrillators of the Primedic™ HeartSave series PDF, 3MB, File does not meet accessibility standards Date: 10. November 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03701/08

Field Safety Notice of the Giraffe Omnibed incubator from GE Healthcare PDF, 79KB, File does not meet accessibility standards Date: 10. November 2008 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 01489/08

Field Safety Notice concerning a software update of the automated external defibrillators from Cardiac Science Corporation PDF, 906KB, File does not meet accessibility standards Date: 10. November 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04041/08

Recall of the defibrillation electrodes from ConMed Corporation PDF, 647KB, File does not meet accessibility standards Date: 10. November 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04080/08

Corrective action / Recall of Oxoid Germany - Thermo Fisher Scientific for PB5008A PDF, 596KB, File does not meet accessibility standards Date: 07. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03963/08

Corrective action / Recall of Oxoid Germany PDF, 46KB, File does not meet accessibility standards Date: 07. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03962/08