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Recall of Marrow-Cut Biopsy Needles from Somatex Medical Technologies PDF, 100KB, File does not meet accessibility standards Date: 09. November 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02618/06

Information about Lithostar Modularis Vario from Siemens Medical Solutions PDF, 41KB, File does not meet accessibility standards Date: 09. November 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02950/06

Information about B|Braun Space Perfuso from B. Braun Melsungen PDF, 56KB, File does not meet accessibility standards Date: 07. November 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02686/06

Recall of Safil violett 0 (3,5) (lot number 1‑4133) from Aesculap PDF, 30KB, File does not meet accessibility standards Date: 07. November 2006 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 03060/06

Corrective action for the INRatio System of Hemosense PDF, 62KB, File does not meet accessibility standards Date: 06. November 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01001/06

Recall of the products „Legion Offset Coupler Trials“ from Smith&Nephew PDF, 107KB, File does not meet accessibility standards Date: 03. November 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02898/06

Corrective action for Calibrator f.a.s. from Roche PDF, 76KB, File does not meet accessibility standards Date: 03. November 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02360/06

Information concerning two defects in Datex-Ohmeda S/5 iCentral software version L-NET05 4.2 from GE Healthcare Technologies PDF, 48KB, File does not meet accessibility standards Date: 03. November 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02987/06

Corrective action for Elecsys Folate II on Elecsys 2010 systems from Roche PDF, 57KB, File does not meet accessibility standards Date: 31. October 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02466/06

Corrective action for the BD™ BBL™ Staphyloslide Latex Test from Becton Dickinson PDF, 48KB, File does not meet accessibility standards Date: 31. October 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02484/06

Recall of the Instant-View Troponin I WB/Serum Cassettes from Alfa Scientific Designs PDF, 38KB, File does not meet accessibility standards Date: 31. October 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01237/06

Recall of TC-100 bone screws from Smith & Nephew PDF, 36KB, File does not meet accessibility standards Date: 31. October 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03098/06

Recall of the cannulated drill bits from Newdeal PDF, 21KB, File does not meet accessibility standards Date: 31. October 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02817/06

Recall of Bremer Halo and Skull Pin products from DePuy PDF, 40KB, File does not meet accessibility standards Date: 31. October 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03155/06

Recall of different Amplatzer® Devices from AGA Medical PDF, 66KB, File does not meet accessibility standards Date: 27. October 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02938/06

Information for the ophthalmologic examination unit Doms Concentric from Doms Eye-Technology PDF, 331KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02544/06

Recall of Interlocking Detachable Coils for Occlusion from Boston Scientific PDF, 174KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03061/06

Recall of the REFSTAR™ External Reference Patches from Biosense Webster PDF, 74KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02857/06

Information concerning all Treatment-versions 8.0.15 and below from Varian PDF, 376KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02942/06

Information concerning the High Energy Clinacs from Varian PDF, 104KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03043/06

Corrective action and recall for the Cystic Fibrosis v3 Genotype Assay from Celera Diagnostics PDF, 84KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02279/06

Recall of CK-NAC FS and CK-MB FS reagents from DiaSys PDF, 68KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02711/06

Information from Stryker concerning the recall of batteries used in Dell Laptops Model D800 PDF, 131KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02738/06

Maintenance instructions for the mobile hoist Victor with scale, type 3000 N2 from Handi-Move PDF, 46KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00161/06

Recall of the SealGuard™ Tracheosoft™ and SealGuard™ Tracheosoft™ PERC™ tracheostomy cannulas from Tyco PDF, 108KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02481/06

Recall of Syphilitop Optima with the lot number 24012 from Biorepair Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02756/06

Corrective action of the Advia Chemistry Systems 1200/1650 and 2400 from Bayer PDF, 185KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02813/06

Corrective action and recall for the m2000sp system from Abbott PDF, 366KB, File does not meet accessibility standards Date: 24. October 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02710/06