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Information concerning the modification of software version 4.29 and the renal replacement therapy device Octo Nova® of the company MeSys GmbH PDF, 108KB, File does not meet accessibility standards Date: 24. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02080/07

Recall of electrode belts of the LifeVest-Systems WCD 3000 of ZOLL Lifecor Corporation PDF, 56KB, File does not meet accessibility standards Date: 24. August 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02581/07

Recall for the Dade Actin Activated Cephaloplastin Reagent (Lot-Number 537148) of Dade Behring PDF, 35KB, File does not meet accessibility standards Date: 23. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02874/07

Information concerning possible dysfunction of the auto start mode for bipolar coagulation of Integra LifeSciences PDF, 49KB, File does not meet accessibility standards Date: 23. August 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02348/07

Corrective action of Roche for Stago STA Compact and STA Compact CT analyzers Date: 22. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02601/07

Recall of microkeratome devices Zyoptix XP Epi Separator and Zyoptix XP Epi Head of the manufacturer Bausch & Lomb. PDF, 41KB, File does not meet accessibility standards Date: 22. August 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02251/07

Recall of Disposable Twist Drill from Biomet 3i PDF, 40KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02007/07

Information about the Clinical Information Center (CIC) Pro from GE Healthcare Technologies PDF, 62KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02832/07

Information concerning the recall of laser devices EndoSet and EndoFiber of the company Asclepion Laser Technologies GmbH PDF, 38KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02442/07

Information concerning the BV Pulsera and Endura Release 2 systems of Philips Medizin Systeme GmbH PDF, 29KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02798/07

Recall of specific lot numbers of the IV Fluid Administration and Irrigation Sets for the Level-1-System from Smiths Medical Deutschland PDF, 39KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03092/06

Recall of the products BD Visc Viscoelastic Solution from Becton Dickinson PDF, 129KB, File does not meet accessibility standards Date: 20. August 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02425/07

Information of remote controlled X-ray systems from Philips Medical Systems PDF, 54KB, File does not meet accessibility standards Date: 17. August 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00144/06

Information about specific blood bag systems from Fenwal, Inc. PDF, 43KB, File does not meet accessibility standards Date: 17. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01883/07

Information concerning the Ambu PEEP 10 reusable valves from Ambu A/S PDF, 264KB, File does not meet accessibility standards Date: 15. August 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00570/07

Information concerning the Level 1 H-1200 and Level 1 H-31B Air Detector acessory from Smiths Medical PDF, 173KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02470/07

Corrective action for the rapid AST testing by means of the Micronaut-SB product line of Merlin Diagnostika PDF, 21KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02579/07

Corrective action for AxSym Digoxin III reagent from Abbott PDF, 39KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02725/07

Recall of Vidas Estadriol from BioMèrieux PDF, 55KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02778/07

Field Safety Notification concerning the Synchromed EL pump motor from Medtronic PDF, 286KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02528/07

Recall of specific vessel cannulae from Maquet PDF, 50KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02315/07

Recall of the Premier Edge MVR 19g Knife and the Premier Edge MVR 20g Knife from OASIS Medical PDF, 168KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02129/07

Information concerning the Disposable Multi Absorber Canister with the EZchange Module from GE Healthcare PDF, 79KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02795/07

Corrective action of the Flex One Suction Hard Canister CF0200 from Cardinal Health PDF, 69KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02227/07

Information about the potential risk and effects of overcharging the internal batteries from Maquet PDF, 98KB, File does not meet accessibility standards Date: 14. August 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02467/07

Recall of the Groove Power Wheelchairs with Quickie Enhanced Display from Sunrise Medical PDF, 242KB, File does not meet accessibility standards Date: 13. August 2007 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02197/07

St. Jude Medical recalls Cardiac Positioning System CPS Direct SL, slittable CRT lead delivery tools PDF, 36KB, File does not meet accessibility standards Date: 10. August 2007 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00956/07

Corrective action of all lot numbers of the product Streptatest from milenia biotec PDF, 64KB, File does not meet accessibility standards Date: 10. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01762/07

Recall of the alternating pressure overlays AS3N and AS3 from Novacare PDF, 44KB, File does not meet accessibility standards Date: 10. August 2007 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02308/07