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14,962 results

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Recall for Surgical Cutters according to Lindemann, Hager & Meisinger PDF, 54KB, File does not meet accessibility standards Date: 14. September 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02800/09

Recall for Renegade Fiber Braided Microcatheter, Renegade Hi-Flo Microcatheter and Renegade Hi-Flo Microcatheter Kits, Boston Scientific PDF, 2MB, File does not meet accessibility standards Date: 14. September 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03222/09

Safety Notice for Hi-Art System, TomoTherapy PDF, 79KB, File does not meet accessibility standards Date: 11. September 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02967/09

Corrective action for Immulite 2000 / 2500 Androstenedione, Siemens PDF, 31KB, File does not meet accessibility standards Date: 11. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03224/09

Safety Notice for Philips IntelliVue Clinical Information Portfolio Release D.0, D.02 and Philips Care Vue Chart Release C.0 PDF, 289KB, File does not meet accessibility standards Date: 11. September 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01306/09

Recall for Ambix activ ambulatory Set and Ambix activ stationary Set, Fresenius Kabi PDF, 17KB, File does not meet accessibility standards Date: 11. September 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02882/09

Safety Notice for Custom Paks, Alcon PDF, 42KB, File does not meet accessibility standards Date: 10. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03391/08

Safety Notice for Dimension Vista® System Software Version 3.2.1 or earlier and Dimension Vista® Flex® reagent cartridges, Siemens PDF, 98KB, File does not meet accessibility standards Date: 10. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02643/09

Recall for Restoration Modular cone Bodies, Stryker PDF, 138KB, File does not meet accessibility standards Date: 10. September 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01363/09

Recall for NOVOCART® 3D Pin FR736, Aesculap PDF, 70KB, File does not meet accessibility standards Date: 10. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03230/09

Safety Notice for WaveScan Offline Programming Module (OPM), AMO Germany GmbH PDF, 206KB, File does not meet accessibility standards Date: 09. September 2009 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02991/09

Safety Notice for Innova 2121IQ, 3131IQ, 2100IQ, 3100IQ and 4100IQ, GE Healthcare PDF, 68KB, File does not meet accessibility standards Date: 09. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03179/09

Safety Notice for Innova 2000, 3100 and 4100 cardiovascular X-ray systems, GE Healthcare PDF, 136KB, File does not meet accessibility standards Date: 09. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03173/09

Important Notice for Quick-Type TM for Lifematch TM Update CD, Tepnel Lifecodes Date: 09. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02924/09

Information for ReFacto AF Laboratory Standard, Wyeth PDF, 218KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02858/09

Corrective action for D.light operating lamps, DKL Chairs GmbH PDF, 99KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 01236/09

Safety Notice for Ventri, GE Medical Systems PDF, 48KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02977/09

Recall for 4.00 Direct measuring Gauges, Smith & Nephew PDF, 54KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02694/09

Safety Notice for Acrobat 2000, Ondal Industrietechnik GmbH PDF, 13KB, File does not meet accessibility standards Date: 08. September 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02060/09

Recall for Neuron Delivery Catheter 0.053, Penumbra PDF, 90KB, File does not meet accessibility standards Date: 07. September 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02740/09