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14,982 results

Results per page: 10 20 30

Corrective action for Dimension® Clinical Chemistry Systems Dimension TACR Flex reagent cartridge, Siemens PDF, 34KB, File does not meet accessibility standards Date: 20. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02252/13

Corrective action for Liaison® Control Biotrin Parvovirus B19 IgM, Diasorin PDF, 109KB, File does not meet accessibility standards Date: 20. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07115/13

Corrective action for Campylobacter CCDA selective medium, Thermo Fisher PDF, 108KB, File does not meet accessibility standards Date: 20. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07469/13

Corrective action for RAPIDLyte Arterial Blood Sampling 3 ml Line Draw Syringes, Siemens PDF, 27KB, File does not meet accessibility standards Date: 20. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00020/14

Urgent Safety Notice for the Duowire™ guidewire, Coloplast PDF, 87KB, File does not meet accessibility standards Date: 20. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00006/14

Recall of one lot of the surgical suture MONOPLUS VIOLET o (3.5) 90 cm, B. Braun Surgical PDF, 3MB, File does not meet accessibility standards Date: 20. January 2014 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 07899/13

Recall of certain lots of the Inzii 12/15mm retrieval system, Applied Medical PDF, 415KB, File does not meet accessibility standards Date: 20. January 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - precision instruments for gastrointestinal and urological endoscopy and hysteroscopy
Reference 06570/13

Corrective action for BacT/Alert PF PLUS and FA Plus Culture Bottles, bioMérieux PDF, 120KB, File does not meet accessibility standards Date: 20. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07132/13

Corrective action for HbA1c liquidirect, Human PDF, 46KB, File does not meet accessibility standards Date: 17. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07670/13

Lot Recall of suprapubic catheter kits, Urotech GmbH PDF, 93KB, File does not meet accessibility standards Date: 17. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 06872/13

Safety Notice for the Precision 500D, Precision MPI and Precision RXI X-ray imaging systems, GE Healthcare PDF, 58KB, File does not meet accessibility standards Date: 17. January 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00062/14

Lot Recall of Sengstaken-Blakemore tube and ENDOGUIDE Guide wire, Teleflex PDF, 355KB, File does not meet accessibility standards Date: 17. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - probes
Reference 07969/13

Urgent Safety Notice for the Hemolung Cartridge Kit, ALung Technologies PDF, 1MB, File does not meet accessibility standards Date: 17. January 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07383/13

Safety Notice for the Radiation Therapy Simulators of type SimView™ NT, Siemens Healthcare PDF, 53KB, File does not meet accessibility standards Date: 17. January 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy simulator
Reference 08001/13

Recall of Laparoscopic BiClamp handles, ERBE Elektromedizin GmbH PDF, 86KB, File does not meet accessibility standards Date: 17. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00060/14

Urgent Safety Notice for the Philips Expression Information Portal (IP5), Philips Healthcare PDF, 108KB, File does not meet accessibility standards Date: 17. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07618/13

Important Safety Notice for the XIO RTP System, IMPAC Medical Systems PDF, 136KB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 07967/13

Corrective action for Total IgE on Immulite® 1000, Immulite® 2000 and Immulite® 2000 XPi, Siemens PDF, 100KB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00017/14

Corrective action for Dimension® TACR Flex® Reagent Cartridges, Siemens PDF, 69KB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07258/12

Corrective action for androstenedione on Immulite® 1000, Immulite® 2000 and Immulite® 2000 XPi, Siemens PDF, 25KB, File does not meet accessibility standards Date: 16. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00022/14