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Baxter recalls infusion extension sets PDF, 77KB, File does not meet accessibility standards Date: 16. February 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00043/06

Guidant recalls the implantable pacemaker models Pulsar, Pulsar Max, Pusar Max II, Discovery, Discovery II, Meridian,Virtus Plus II, Intelis II and Contak TR PDF, 363KB, File does not meet accessibility standards Date: 16. February 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01750/05

Recall of the thermometer OMRON ProTemp - MC600 PDF, 17KB, File does not meet accessibility standards Date: 16. February 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02810/05

Connection Problems with Lifepak 500 defibrillators from Medtronic PDF, 32KB, File does not meet accessibility standards Date: 16. February 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00295/06

Problem with Ultrasound scanner Aplio and Xario from Toshiba PDF, 102KB, File does not meet accessibility standards Date: 13. February 2006 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03345/05

An anomaly has been identified in Eclipse and Vision from Varian Medical Systems PDF, 165KB, File does not meet accessibility standards Date: 13. February 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03030/05

Corrective action of Biomerieux for BacT/Alert® and BacT/View® systems PDF, 204KB, File does not meet accessibility standards Date: 10. February 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00281/06

Preventive Maintenance Instructions for the 3D-TOP Ceiling Stand, Siemens PDF, 61KB, Date: 20. January 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03169/05

Guidant recalls Contak Renewal and Contak Renewal 2 PDF, 1MB, Date: 20. January 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02284/04

Missing wax plugs in the Microbiology Brushes from Boston Scientific PDF, 291KB, Date: 20. January 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00025/06

Risk in the use of 850 Humidification Systems from Fisher & Paykel with non original accessories PDF, 29KB, Date: 19. January 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01513/05

Corrective action and recall for Coulter LH 700 und Gen•S Haematology analyzers, Beckman PDF, 216KB, Date: 19. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00049/06

Recall of Biermann for the Immulite 2000 Testosteron Assay PDF, 63KB, Date: 19. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00045/06

Coloplast recalls the Contreet Non-Adhesive Foam wound dressing PDF, 60KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 02811/05

Safety instruction for the CODMAN High Speed Drill System from Ethicon PDF, 427KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01680/05

MediTrade informs about the distribution of fakes PDF, 351KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03365/05

Exchange of all Nihon Kohden QI-403P Interface PDF, 56KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03363/05

Risks when using the povidon-iodine containing MiniCap/OptiCap disconnect caps from Baxter PDF, 173KB, Date: 13. January 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03332/05

Corrective action and Recall for Omni S system versions 2, 4 and 6 with CO-oximetry, Roche PDF, 104KB, Date: 10. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02832/05

Notification of issues with the Accura System for Blood Filtration from Baxter PDF, 183KB, Date: 09. January 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03034/05

Exatech recalls the Optetrak Cemented Finned Tibial Trays PDF, 44KB, Date: 03. January 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03407/05

The Mammendorfer Institut recalls the ECG Boy PDF, 28KB, Date: 02. January 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02357/05

Corrective action of Becton Dickinson for BD Logic glucometers PDF, 170KB, Date: 02. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03358/05

Corrective action of Abbott Medisense for Precision Xtra and Precision Xtra OK glucometers PDF, 123KB, Date: 02. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03354/05

Corrective action of Roche for Elecsys Troponin T PDF, 80KB, Date: 02. January 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03361/05

Safety risk in the wheel suspension of the three-wheeled chair Cheetah from R82 PDF, 169KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02987/05

Additional warning from Baxter BioScience for the product CoSeal PDF, 49KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03130/05

Risk of breakage in the backrest of the beds Arminia 2, Westfalia 3, Theutonia 3 and Fortuna from Burmeier PDF, 19KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02766/05

Corrective action of the ERBE Helix Hydro-Jet PDF, 77KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01470/05

Problems with the Neonatal Ventilator Baylog 8000plus from Dräger PDF, 63KB, Date: 30. December 2005 Topics: Medical devices Type: Customer information

Reference 03343/05