BfArM - Federal Institute for Drugs and Medical Devices

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OrbusNeich recalls Constant SDS PDF, 33KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01964/05

Hill-Rom informs about battery failure in the hand control of the mattress system Duo PDF, 79KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01986/05

Ciba Vision recalls the contact lens care product Clerz PDF, 36KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01764/05

Corrective action of Lifepak 500 AED from Medtronic PDF, 52KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01074/05

Corrective action for the RIA Unconjugated Estriol Kit, Beckman Coulter PDF, 60KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02001/05

Corrective action and recall of Sysmex and Dade Behring for Sysmex CA-1500, CA-7000 and CA-500 instruments PDF, 144KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01440/05

Problems with the ViewForum release 3.4L1 from Philips PDF, 43KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01423/05

Miehtke recalls severeal lots of their control reservoir PDF, 66KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01809/05

Fractures of the backrest tubes of the folding wheelchair Action³ from Invacare PDF, 93KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01504/04

Guidant recalls the HEARTSTRING II Aortic Cutters PDF, 101KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Reference 01647/05

Corrective action of Beckman Coulter for Access Immunosystems Unconjucated Estriol Calibrators PDF, 183KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01912/05

Corrective action of Roche for Accu-Chek Active PDF, 62KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01890/05

Corrective action and recall of Cepheid Europe for DX Software Smartcycler PDF, 56KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01948/05

Recall of Mast Diagnostics for the Mast ESßL Set PDF, 35KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01916/05

Tyco recalls Tear Away Introducer Sheaths PDF, 91KB, Date: 04. August 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01655/05

Recall of BioMerieux for MRSA ID agar PDF, 142KB, Date: 04. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01852/05

Recall and corrective action of Beckman Coulter for MXP software versions 1.0 and 2.0 for FC500 systems PDF, 274KB, Date: 04. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01859/05

Corective action of the Digital Mammographiesystem MAMMOMAT NovationDR from Siemens PDF, 63KB, Date: 29. July 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01276/05

Incorrect couch position that are displayed on the monitor of Brilliance CT scanners from Philips PDF, 822KB, Date: 29. July 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01521/05

Zimmer GmbH informs about a recall of the instruments Revitan Straight and Curved Disassembly Sleeve PDF, 62KB, Date: 29. July 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01450/05

Problems with the Bloom Programmable Stimulator from Fisher Imaging PDF, 24KB, Date: 29. July 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01147/05

Baxter informs about several issues of application of the volumetric infusion pump Collegue PDF, 238KB, Date: 29. July 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01004/05

Recall and corrective action of Dade Behring for Coagulation Factor VIII Deficient Plasma PDF, 222KB, Date: 27. July 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01597/05

Corrective action of Abbott for FreeStyle™, Freestyle Mini™, Precision Xtra™ and Precision Xceed™ blood glucometers PDF, 119KB, Date: 27. July 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01461/05

Zimmer recalls Innex anchorage stem PDF, 56KB, Date: 25. July 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01060/05

Zimmer recalls two lots of the Dynesys Torque Driver 450 PDF, 64KB, Date: 25. July 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00943/05

Medicel recalls the Viscoject Cartridge Sets LP604240M PDF, 43KB, Date: 25. July 2005 Topics: Medical devices Type: Customer information

Reference 01333/05

Laerdal Medical recalls an adaptor cable PDF, 63KB, Date: 25. July 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00845/05

Argon recalls the 10cc/12cc Sterile or Non-Sterile Control Syringes and Sterile or Non-Sterile Kits with Control Syringes PDF, 164KB, Date: 25. July 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01578/05

TheraSelect recalls the Altair 16G PDF, 35KB, Date: 25. July 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01369/05