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Corrective action / Recall for the Modular glucose method (GLUCm) on Synchron LX and UniCel DxC Systems, Beckman Coulter PDF, 87KB, File does not meet accessibility standards Date: 12. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01790/10

Safety Notice for SQRX®PulseGenerator, Cameron Health PDF, 49KB, File does not meet accessibility standards Date: 12. August 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01680/11

Safety Corrective Action for ReNew Long Fenestrated Grasper, Microline Surgical Inc. PDF, 1MB, File does not meet accessibility standards Date: 12. August 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03605/11

Recall of the V40 Unipolar Hip Heads, Stryker PDF, 88KB, File does not meet accessibility standards Date: 12. August 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02347/11

Corrective action for HemoCue Glucose 201 RT and HemoCue Glucose 201 DM RT, HemoCue PDF, 533KB, File does not meet accessibility standards Date: 11. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03542/11

Corrective action for PRISCA 5.0, Siemens PDF, 29KB, File does not meet accessibility standards Date: 11. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03558/11

Recall for the Architect C-Peptide Reagent, Abbott PDF, 45KB, File does not meet accessibility standards Date: 10. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02443/11

Recall for ADVIA Chemistry Gentamicin_2 (GENT_2) and Valproic Acid_2 (VPA_2) Reagent, Siemens PDF, 108KB, File does not meet accessibility standards Date: 10. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03594/11

Recall for Dyonics Power Keyless Chuck, Smith & Nephew PDF, 45KB, File does not meet accessibility standards Date: 09. August 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01374/11

Safety Notice for Vital Signs Monitor, Spacelabs Medical PDF, 34KB, File does not meet accessibility standards Date: 09. August 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03474/11

Safety Notice for Philips Intellivue Clinical Information Portfolio Releases D.03, E.0 und E.01, Philips Healthcare PDF, 52KB, File does not meet accessibility standards Date: 09. August 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03422/11

Urgent Safety Notice: Correct use of measuring spoons, Joma GmbH PDF, 355KB, File does not meet accessibility standards Date: 08. August 2011 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03223/11

Recall for V-Max® 6-Inch Beveled Bone Access Needle, DePuy PDF, 48KB, File does not meet accessibility standards Date: 08. August 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03518/11

Recall for SenSura® and Assura® colostomy bags, Coloplast PDF, 49KB, File does not meet accessibility standards Date: 05. August 2011 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03443/11

Lot Recall for CooperSurgical Mystic II Vacuum Assisted Delivery Products, Cooper Surgical Inc. PDF, 165KB, File does not meet accessibility standards Date: 05. August 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03515/11

Urgent Safety Notice for Keeler Cryomatic Probes, Keeler Ltd. PDF, 429KB, File does not meet accessibility standards Date: 05. August 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02897/11

Recall regarding Operating Table TruSystem 7500 / ARTIS, Trumpf Medizin Systeme GmbH + Co. KG PDF, 40KB, File does not meet accessibility standards Date: 04. August 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02263/11

Corrective action for Bio-Rad Whole Blood Controls, Alba Bioscience PDF, 71KB, File does not meet accessibility standards Date: 04. August 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03199/11

Lot Recall of Radiation Shields flat for the Intrabeam Radiosurgery Treatment system, Carl Zeiss Meditec PDF, 43KB, File does not meet accessibility standards Date: 04. August 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03232/11

Recall for Arteriofix V Arterial catheter kits, B. Braun Melsungen PDF, 63KB, File does not meet accessibility standards Date: 03. August 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01455/11

Urgent Safety Information for the EnduRo Knee-System, Aesculap PDF, 110KB, File does not meet accessibility standards Date: 03. August 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02437/11

Safety Notice concerning the correct use of Resolution II Clip, Boston Scientific PDF, 30KB, File does not meet accessibility standards Date: 03. August 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03455/11

Important Safety Notice for XiO, Elekta CMS Software PDF, 37KB, File does not meet accessibility standards Date: 03. August 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02380/11

Safety Notice for A-dec-311-articulating headrest, A-dec Dental UK Ltd. PDF, 99KB, File does not meet accessibility standards Date: 02. August 2011 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02828/11

Recall for MEDSTREAM® Implantable Drug Infusion Pumps, Codman PDF, 32KB, File does not meet accessibility standards Date: 02. August 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03363/11

Safety Notice for all HL 20 Twin Pump Modules - Release Version 11, Maquet Getinge Group PDF, 62KB, File does not meet accessibility standards Date: 02. August 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03212/11

Lot Recall for Coseal Surgical Sealant, BAXTER PDF, 47KB, File does not meet accessibility standards Date: 02. August 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03467/11

Safety Notice for Flexitron HDR Afterloader, Nucletron PDF, 104KB, File does not meet accessibility standards Date: 02. August 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02414/11

Safety Notice for the AMO STAR S4 IR Excimer Laser System, Abbott Medical Optics Inc. PDF, 159KB, File does not meet accessibility standards Date: 01. August 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03159/11

Urgent Safety Alert for CADD®-Solis Ambulatory Infusion Pumps, Smiths Medical International Ltd. PDF, 59KB, File does not meet accessibility standards Date: 01. August 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03190/11