BfArM - Federal Institute for Drugs and Medical Devices

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14,972 results

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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

BfArM’s assessment concerning oxygen concentrators Date: 28. September 2011 Topics: Medical devices Type: Article

Survey on the recommendation addressed to the local competent authorities concerning oxygen concentrators

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

Corrective action for G8 Hemoglobin F&A2 Calibrator and Hemoglobin F and A2 Control, TOSOH Bioscience PDF, 160KB, File does not meet accessibility standards Date: 26. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04109/11

Recall for MKONA-Z and MKONA-1, Privates Institut für Immunologie und Molekulargenetik PDF, 288KB, File does not meet accessibility standards Date: 26. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04262/11

Safety Notice for several sets intended to be used with infusion pumps, Unomedical A/S PDF, 743KB, File does not meet accessibility standards Date: 23. September 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03931/10

Lot Recall of AVAIRA Toric contact lenses, CooperVision PDF, 837KB, File does not meet accessibility standards Date: 23. September 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03948/11

Safety Notice for Synchromed II Implantable Drug Infusion Pumps, Medtronic PDF, 46KB, File does not meet accessibility standards Date: 23. September 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 04254/11

Recall of all Pleura Flow Catheter Systems of the manufacturer Xeridiem Medical Devices, Clear Catheter Systems PDF, 41KB, File does not meet accessibility standards Date: 23. September 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01852/11

Recall for the Endoplege Coronary Sinus Catheter Kit, Edwards Lifesciences PDF, 65KB, File does not meet accessibility standards Date: 22. September 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02863/11

Corrective action for Advia 120/2120/2120i Hematology Systems, Siemens PDF, 29KB, File does not meet accessibility standards Date: 22. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04334/11

Recall for Clinical Chemistry Alkaline Phosphatase, Abbott PDF, 80KB, File does not meet accessibility standards Date: 21. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04033/11