BfArM - Federal Institute for Drugs and Medical Devices

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Recall for Medi-Vac Non-Conductive Suction Tubings, Cardinal Health PDF, 46KB, File does not meet accessibility standards Date: 08. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03033/10

Safety Notice for IntelliVue Patient Monitors, Philips PDF, 115KB, File does not meet accessibility standards Date: 08. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03003/10

Lot Recall for suction catheters with funnel connectors, Unomedical PDF, 189KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02556/10

Recall of a limited number of the automated external defibrillators (AEDs) HeartStart FRx 861304, HeartStart HS1 M5066A and HeartStart Home M5068A, Philips Healthcare PDF, 191KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02003/10

Field Safety Notice concerning the Flexible Probe with Blocking Washer, GM11002420, Varian Medical Systems PDF, 118KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01985/10

Safety Notice for INNOTEST ß-AMYLOID(1-42), Innogenetics PDF, 62KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02082/10

Recall for ARCHITECT Sirolimus Reagent, list no. 01L76-25, lot no. 80162M100, Abbott PDF, 36KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02024/10

Safety Notice for iVue100, Optovue PDF, 105KB, File does not meet accessibility standards Date: 06. September 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02995/10

Safety Notice for Contasure Needleless, DIMA PDF, 14KB, File does not meet accessibility standards Date: 06. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02270/10

Recall for Impella® 5.0, ABIOMED PDF, 102KB, File is accessible Date: 06. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02414/10

Safety Notice for IGFBP-3 IRMA kits, Beckman Coulter PDF, 87KB, File is accessible Date: 03. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03085/10

Recall for Disposable Scope Warmer, Stryker PDF, 530KB, File is accessible Date: 03. September 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02543/10

Safety Notice on Easyband Telemetric Gastric Bands, Allergan PDF, 204KB, File is accessible Date: 03. September 2010 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02853/10

Recall of the CUSA NXT Ultrasonic Surgical Aspirator System, Integra LifeSciences PDF, 200KB, File is accessible Date: 03. September 2010 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02649/10

Lot Recall for CT Drainage Set, Direct puncture set with pigtail catheter, OptiMed PDF, 156KB, File is accessible Date: 02. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03063/10

Lot-Recall for „blend-a-dent Super-Haftcreme extra stark und frisch“, PROCTER & GAMBLE PDF, 487KB, File is accessible Date: 02. September 2010 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 03026/10

Safety Notice for MX 8000 IDT 16, Philips PDF, 76KB, File is accessible Date: 02. September 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02975/10

Recall for Captia VZV IgM Kit, Trinity Biotech PDF, 73KB, File is accessible Date: 31. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02708/10

Lot recall for 1•Day Acuvue® TruEye™, Johnson & Johnson Vision Care PDF, 106KB, File is accessible Date: 31. August 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03008/10

Recall for Access Thyroglobulin Antibody II, Beckman Coulter PDF, 142KB, File is accessible Date: 31. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02503/10