BfArM - Federal Institute for Drugs and Medical Devices

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Smith & Nephew recall the sterile wound dressing Opsite Post-Op PDF, 88KB, Date: 08. December 2005 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 02808/05

Recall of Dade Behring for N Latex SAA OQMP PDF, 60KB, Date: 08. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02895/05

Corrective action of Dade Behring for Complement Reagents PDF, 61KB, Date: 08. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02869/05

DePuy Orthopaedics recalls the Acclaim Total Elbow Joint Replacement Implant PDF, 112KB, Date: 05. December 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02985/05

Corrective action on Sola 300 from Dräger PDF, 54KB, File does not meet accessibility standards Date: 05. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02061/05

Otto Bock recalled the powered wheelchairs C1000 and B600 PDF, 84KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02983/05

Recall of Hedstrom Files from Kerr Hawe PDF, 95KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02868/05

Boston Scientific recalls the MAVERIK™ Monorail™ catheter PDF, 99KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02946/05

Corrective action of BioMerieux for ID 32, Rapid ID 32, Rapid ATB and ATB identification strips PDF, 130KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03021/05

Corrective action of Roche for COBAS Ampliprep/COBAS TaqMan tests PDF, 308KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02253/05

Cardiac Science recalls the Powerheard AED G3s PDF, 96KB, Date: 02. December 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01354/05

Advanced Sterilization Products (ASP) recalls the vaporizer plates PDF, 102KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02490/05

Recall of Guidant heart pacemakers Insignia and Nexus PDF, 142KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02387/05

Therapy failure of the Guidant ICD Contak Renewal and Renewal PDF, 114KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01258/05

Break in communication between the Desktop Premium Therapy software from Elekta and its database results PDF, 102KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02905/04

No-output condition of Ela Medical pacemakers Symphony und Rhapsody PDF, 45KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01512/04

Recall of St. Jude Medical ICD Photon, Photon Micro and Atlas PDF, 203KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02528/05

Software problem with Active Breathing Coordinator from Elekta PDF, 27KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02493/05

Anomaly in VARiS Vision RTP Exchange from Varian PDF, 44KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02447/05

Zimmer recalls the product Sirus Step Reamer PDF, 340KB, Date: 24. November 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02739/05