BfArM - Federal Institute for Drugs and Medical Devices

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Tyco recalls the Shiley FlexTra Tracheostomy Tubes PDF, 59KB, Date: 29. December 2004 Topics: Medical devices Type: Customer information

Reference 02928/04

Corrective action of Olympus Diagnostica for Olympus AU400, AU600, AU640, AU2700 and AU5400 series PDF, 53KB, Date: 29. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03050/04

William Cook recalls some tracheostomy-sets PDF, 117KB, Date: 29. December 2004 Topics: Medical devices Type: Customer information

Reference 02982/04

Exchange of adjustment clips in walking aids from Ortopedia PDF, 37KB, Date: 28. December 2004 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02385/04

Corrective action for ProC Global, Dade Behring PDF, 58KB, Date: 28. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02890/04

Recall of Dade Behring for Dade Actin PDF, 35KB, Date: 28. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02833/04

Corrective action of DPC Biermann for Immulite 2500 Homocystein PDF, 111KB, Date: 28. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02502/04

Corrective Action of Abbott for Architect B12 PDF, 84KB, Date: 27. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03020/04

Corrective action of Abbott for Murex HSV PDF, 86KB, Date: 23. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02959/04

Corrective action of Roche for SnapPak PDF, 78KB, Date: 23. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02812/04

Corrective action of Becton Dickinson for FACSCanto Flow cytometer PDF, 59KB, Date: 23. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02499/04

Corrective action for Coulter UniCel DxI, Beckman Coulter PDF, 107KB, Date: 23. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02696/04

Recall of the NE330R Columbus/E.Motion Femural Inserter Extractor from Aesculap PDF, 136KB, Date: 21. December 2004 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02721/04

Medtronic recalls the DLP VAD Cannula for Ventricular Assist and the Cardio Kits C390601A, C391102A, M850313A PDF, 42KB, Date: 21. December 2004 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02223/04

Recall of Remel Europe for Wellcogen Bacterial Antigen Kit PDF, 64KB, Date: 21. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02978/04

Corrective action on lubricant diffuser cartridges from Medtronic PDF, 51KB, Date: 21. December 2004 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02675/04

Corrective action for Coulter AcT diff 2 hematology analyzers, Beckman Coulter PDF, 102KB, Date: 21. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02950/04

Corrective action for BD Microtainer tubes, Becton Dickinson PDF, 236KB, Date: 21. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02769/04

Roche recalls the Omni S S1 Rinse solution PDF, 60KB, Date: 21. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02731/04

Corrective action of Beckman Coulter for Synchron Systems Lipase Reagent PDF, 58KB, Date: 21. December 2004 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02589/04