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Recall of the products TOM PLUG FOR 01-15400/401 from Stryker PDF, 75KB, File does not meet accessibility standards Date: 25. September 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02625/07

Software discrepancy of the Verify and Record systems IMPAC MOSAIQ version 1.20L1-P4 from Elekta Limited Date: 25. September 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03083/07

Recall of the Dimension clinical chemistry system Total triiodothyronine (T3) Flex reagent cartridge from Dade Behring PDF, 30KB, File does not meet accessibility standards Date: 25. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03300/07

Corrective action for the Dimension Vista System V-Lyte Integrated Multisensor from Dade Behring PDF, 27KB, File does not meet accessibility standards Date: 25. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03299/07

Information concerning the e.motion and Columbus Femural Components from Aesculap PDF, 54KB, File does not meet accessibility standards Date: 24. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03327/07

Recall of Arm positioning devices (1001. 44CO/DO/EO/FO) and Elbow support devices (1004. 23CO) from Maquet PDF, 405KB, File does not meet accessibility standards Date: 24. September 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02991/07

Recall of the Universal Sling Bar with the product numbers 3156075, 3156085 and 3156095 from Liko PDF, 56KB, File does not meet accessibility standards Date: 19. September 2007 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02268/07

Recall of the Renegade™ Hi-Flo Microcatheter Kit from Boston Scientific PDF, 104KB, File does not meet accessibility standards Date: 19. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03281/07

Corrective action for Vidas C. difficile Toxin A&B from of bioMérieux PDF, 66KB, File does not meet accessibility standards Date: 19. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03278/07

Recall of the AED 20 defibrillators from Welch Allyn PDF, 297KB, File does not meet accessibility standards Date: 19. September 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02985/07

Product Safety Notification concerning the systems Precision Rxi and Precision e from GE Healthcare PDF, 76KB, File does not meet accessibility standards Date: 17. September 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00144/06

Corrective action for Precision Xceed blood glucose monitoring products from Abbott PDF, 365KB, File does not meet accessibility standards Date: 17. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03006/07

Recall of the 200 ml disposable syringes manufactured by Nemoto Kyorindo PDF, 27KB, File does not meet accessibility standards Date: 14. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02253/07

Recall of the Mechanical Heart valves Advantage® from Medtronic PDF, 245KB, File does not meet accessibility standards Date: 14. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01763/07

Corrective action of the RD/Hitachi 902/904/911/912, RD Hitachi/917 Modular P and Modular P for the test glucose in haemolysate from Roche PDF, 183KB, File does not meet accessibility standards Date: 13. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00323/07

Extension of the recall of certain lots of the Mach I™ Guide Catheters from Boston Scientific PDF, 304KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02557/07

Recall of the Colorado 2 Locking Nuts from Medtronic PDF, 231KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03170/07

Recall of the resorbable bone screws Calaxo from Smith & Nephew PDF, 40KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03129/07

Corrective action of the Infinity™ Ammonia Liquid Stable Reagent from Thermo Fisher Scientific PDF, 246KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02871/07

Recall of the guide wires from C.R. Bard GmbH PDF, 78KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03101/07

Recall for ABL77 cal pack lots from Radiometer Copenhagen PDF, 30KB, File does not meet accessibility standards Date: 11. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03100/07

Recall for the Data Innovations Instrument Manager from Beckman Coulter PDF, 171KB, File does not meet accessibility standards Date: 11. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03142/07

Recall for the IGF-I IRMA Kit from Beckman Coulter PDF, 38KB, File does not meet accessibility standards Date: 11. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03140/07

Recall of the Pressure transducers DPT 8003 from Codan pvb Critical Car GmbH PDF, 35KB, File does not meet accessibility standards Date: 11. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02994/07

Recall for the Trinity Biotech Captia Varicella-Zoster (VZV) IgM from Trinity Biotech PDF, 58KB, File does not meet accessibility standards Date: 10. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02379/07

Corrective action for the Strep A Schnelltest-Streifen and the Strep A Schnelltest-Gerät from Innovacon PDF, 50KB, File does not meet accessibility standards Date: 10. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02577/07

Safety Information concerning the pediatric fitting of hearing instruments INTUIS S Dir and CIELO 2 from Siemens Audiologische Technik GmbH PDF, 44KB, File does not meet accessibility standards Date: 10. September 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02648/07

Recall of Caeruloplasmin NL BINDARID Radial Immunodiffusion Kits from The Binding Site PDF, 112KB, File does not meet accessibility standards Date: 07. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02922/07

Recall of burs, irrigation instruments etc. from ConMed Linvatec PDF, 322KB, File does not meet accessibility standards Date: 06. September 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02915/07