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Corrective action for Galileo Echo, Immucor PDF, 31KB, File does not meet accessibility standards Date: 29. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04321/11

Lot Recall for the 13 Hole Scapula Medial Boarder Plate, ACUMED PDF, 38KB, File does not meet accessibility standards Date: 28. September 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04407/11

Lot Recall of the Trabecular Metal™ Acetabular System Shell without holes, Zimmer PDF, 619KB, File does not meet accessibility standards Date: 28. September 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04338/11

Recall of Flexible Probe with Blocking Washer, Varian medical systems PDF, 129KB, File does not meet accessibility standards Date: 27. September 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04312/11

Recall for MKMTR 1, Privates Institut für Immunologie und Molekulargenetik PDF, 1MB, File does not meet accessibility standards Date: 27. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04355/11

Lot Recall for Breeze Resin Cement, PENTRON CLINICAL PDF, 63KB, File does not meet accessibility standards Date: 27. September 2011 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 03811/11

Safety Notice for the Accent DR dual-chamber pacemaker and the Anthem CRT-P, St. Jude Medical PDF, 61KB, File does not meet accessibility standards Date: 26. September 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 04361/11

Corrective action for BD Multitest CD3/CD16+56/CD45/CD19 with BD Trucount Beads, Becton Dickinson PDF, 59KB, File does not meet accessibility standards Date: 26. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03913/11

Recall of all Duration® packaged product having an expiration date between September 2011 and June 2016, Stryker PDF, 730KB, File does not meet accessibility standards Date: 26. September 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04105/11

Safety Notice for THERAKOS™ CELLEX™ Photopherese System PDF, 59KB, File does not meet accessibility standards Date: 26. September 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04052/11