BfArM - Federal Institute for Drugs and Medical Devices

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Corin Medical recalls the Uniglide Femoral Drills PDF, 53KB, Date: 24. October 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02483/05

Aesculap recommends to check the tibia preparation plateaus PDF, 111KB, Date: 24. October 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02467/05

Recall of Dade Behring for Dade Actin FS PDF, 55KB, Date: 24. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02418/05

Recall of Roche for Elecsys Assay Tips PDF, 164KB, Date: 24. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02522/05

Potential failure with the Image Navigator function of the SIENET COSMOS Workplace from Siemens PDF, 48KB, Date: 19. October 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02329/05

eVent Medical recalls the Inspiration Ventilator System PDF, 121KB, Date: 19. October 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02354/05

Single incident during the use of a flexible implant tube with blind end from Varian PDF, 1MB, Date: 19. October 2005 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02453/05

AGA Medical recalls the AMPLATZER® Duct Occluder PDF, 98KB, Date: 18. October 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02295/05

Advice for electronic wheelchair Allround 960 C, Ortopedia PDF, 44KB, Date: 18. October 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01862/03

Recall of DakoCytomation for HercepTest PDF, 114KB, Date: 18. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02525/05

Boston Scientific recalls Enteryx Procedure Kits and Enteryx Injector products PDF, 289KB, Date: 14. October 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02426/05

Medtronic is replacing older version QUIK-COMBO pacing/defibrillation/ECG cables and Standard paddles PDF, 25KB, Date: 14. October 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02236/05

Recall and corrective action of BioMerieux for Vitek 2 GN ID Test Kits PDF, 60KB, Date: 14. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02439/05

Recall and corrective action of Abbott for Architect c8000 analyzers PDF, 194KB, Date: 14. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02376/05

Recall of Brahms Kryptor Solution 1 PDF, 62KB, Date: 14. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01943/05

Recall and corrective action of Lifescan for OneTouch GlucoTouch blood glucose analyzers PDF, 120KB, Date: 14. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02330/05

Recall of Abbott for CELL-DYN diluent PDF, 150KB, Date: 14. October 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02435/05

Exchange of plates for adjusting camber in wheelchairs model Avantgarde from Bock PDF, 19KB, Date: 13. October 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01113/05

Mislabeling incident with the OptiLock Ports from LeMaitre PDF, 99KB, Date: 13. October 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02353/05

User Information for the Lifepak 500 AED from Medtronic PDF, 61KB, Date: 13. October 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02254/05