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14,972 results

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Batch recall of Optiplug® Cement Restrictors, Integra LifeSciences PDF, 127KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 05678/11

Lot recall for Vancomycin Calibrators (Lot-No. 59391741), ThermoFisher PDF, 48KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 05588/11

Recall for Terumo Sarns Adult Rigid Intracardiac Suckers, Terumo Europe NV PDF, 50KB, File does not meet accessibility standards Date: 20. December 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04697/11

Recall of the device NL8600401 – Non-sterile stainless steel stepdown connector, Integra NeuroSciences PDF, 76KB, File does not meet accessibility standards Date: 16. December 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 05782/11

Safety Notice for the FrameArray Module (of the Optical Guidance Platform), Varian medical systems PDF, 384KB, File does not meet accessibility standards Date: 16. December 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 05698/11

Recall for AIA-PACK ß HCG Calibrator Set, TOSOH Bioscience PDF, 3MB, File does not meet accessibility standards Date: 16. December 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 05501/11

Safety Notice for 4D Structure Merge Tool Option in Eclipse Release 8.5-10 with 4D Planning, Varian medical systems PDF, 440KB, File does not meet accessibility standards Date: 16. December 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 05590/11

Lot Recall of 1 DAY ACUVUE MOIST contact lenses, Johnson & Johnson Vision Care PDF, 63KB, File does not meet accessibility standards Date: 15. December 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 05644/11

Safety Notice concerning Revolution XR/d X-ray Systems, GE Healthcare PDF, 30KB, File does not meet accessibility standards Date: 15. December 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 05605/11

Additional Information: Lot Recall of different dialysis tubing systems, Gambro PDF, 299KB, File does not meet accessibility standards Date: 15. December 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03409/11

Safety Notice for DigitalDiagnost Release 3, Philips PDF, 47KB, File does not meet accessibility standards Date: 15. December 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 05627/11

Safety Notice for Pentax EG-3870UTK Ultrasound video endoscope PDF, 672KB, File does not meet accessibility standards Date: 15. December 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 05024/11

Safety Notice concerning a recall for several lots of SERFAS Energy Probes Super 90S, Stryker PDF, 109KB, File does not meet accessibility standards Date: 14. December 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 05420/11

Safety Notice concerning MammoDiagnost DR X-ray systems, Philips PDF, 128KB, File does not meet accessibility standards Date: 14. December 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 05624/11

Safety Information for Ceragem-E, Ceragem Europe GmbH PDF, 24KB, File does not meet accessibility standards Date: 14. December 2011 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 02540/10

Lot Recall for Creatinine (CREA) Flex reagent cartridges (DF33A), Siemens Healthcare Diagnostics GmbH PDF, 35KB, File does not meet accessibility standards Date: 13. December 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 05635/11

Lot Recall for Dimension Vista Cardiac Troponin I Calibrator (KC 678), Siemens Healthcare Diagnostics GmbH PDF, 35KB, File does not meet accessibility standards Date: 13. December 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 05606/11

Safety Notice for the Norland Illuminatus DXA Software with the DICOM Option, CooperSurgical PDF, 34KB, File does not meet accessibility standards Date: 13. December 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04988/11

Safety Notice for ImmunoCAP Allergen f14 (Soybean), Phadia AB PDF, 41KB, File does not meet accessibility standards Date: 13. December 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 05618/11

Lot Recall for Rüsch Steel Guidewires, Teleflex PDF, 42KB, File does not meet accessibility standards Date: 13. December 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 05497/11