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Recall involving Genesis II Resection Cutting Blocks Size 4 and 5, items 71440116 and 71440118, Smith & Nephew, Inc.
PDF, 73KB, File does not meet accessibility standards
Date: 21. June 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01944/10

Safety Notice for Monitor Suspension Systems type GD60-W, MAVIG PDF, 306KB, File does not meet accessibility standards Date: 08. June 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01892/10

Recall for AVS-TL-Spacer, Stryker PDF, 82KB, File does not meet accessibility standards Date: 08. June 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01880/10

Recall for AB 5000 Console, ABIOMED PDF, 54KB, File does not meet accessibility standards Date: 08. June 2010 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00830/10

Corrective action for the Clinical Chemistry Phosphorus Assay, Abbott PDF, 56KB, File does not meet accessibility standards Date: 08. June 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01887/10

Recall for Aimer Endofemoral, Smith & Nephew PDF, 86KB, File does not meet accessibility standards Date: 08. June 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01787/10

Safety Notice for iCentral and iCentral Clients v5.0.2, GE Healthcare Finland Oy PDF, 64KB, File does not meet accessibility standards Date: 08. June 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01747/10

Safety Notice for ADVIA Centaur Systems Calibrator A, Siemens PDF, 42KB, File does not meet accessibility standards Date: 07. June 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01912/10

Safety Notice for LithoDiagnost and UroDiagnost, Philips PDF, 28KB, File does not meet accessibility standards Date: 07. June 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01750/10

Safety Notice for Innova 2100IQ, 3100, 3100IQ, 4100 and 4100IQ with InnovaIQ-table, GE Healthcare PDF, 66KB, File does not meet accessibility standards Date: 07. June 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01879/10

Safety Notice for Carescape Monitor B850, GE Healthcare PDF, 142KB, File does not meet accessibility standards Date: 04. June 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01746/10

Lot Recall for PhaSeal C70 Infusion Adaptor, Carmel Pharma AB PDF, 40KB, File does not meet accessibility standards Date: 04. June 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01913/10

Safety Notice for Constellation Vision System PDF, 84KB, File does not meet accessibility standards Date: 04. June 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01911/10

Safety Notice for Aespire, Avance, Amingo and ADS180 Anaesthesia Machines, GE Healthcare PDF, 54KB, File does not meet accessibility standards Date: 02. June 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01822/10

Safety Notice for Diagnost 56/66/76, EasyDiagnost and EasyDiagnost Digital with SCP Generator, Philips Healthcare PDF, 28KB, File does not meet accessibility standards Date: 02. June 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01749/10

Safety Notice for C500 S-10 R-NET and other R-Net chairs with ESP, Permobil PDF, 36KB, File does not meet accessibility standards Date: 02. June 2010 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01694/10

Recall for Arrow 4 Fr Peripherally Inserted Central Catheter (PICC) kits, Teleflex Medical PDF, 155KB, File does not meet accessibility standards Date: 01. June 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01870/10

Recall for TruCal ApoA1 calibrator set, Diasys PDF, 85KB, File does not meet accessibility standards Date: 01. June 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01806/10

Recall for IMx Sirolimus Reagent, Abbott PDF, 36KB, File does not meet accessibility standards Date: 01. June 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01793/10

Recall for "Actavis-Mini-Pumpe", Actavis Deutschland GmbH & Co. KG PDF, 152KB, File does not meet accessibility standards Date: 31. May 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01665/10

Lot Recall for LRS ADV, Micrometric Translation-Angulation Clamp, Orthofix PDF, 346KB, File does not meet accessibility standards Date: 31. May 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01785/10

Safety Notice for FL400 Fluorescence Imaging Feature for M720 OH5, Leica PDF, 79KB, File does not meet accessibility standards Date: 31. May 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01760/10

Safety Notice for Minstrel lift devices, ArjoHuntleigh PDF, 179KB, File does not meet accessibility standards Date: 31. May 2010 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01456/10

Recall for 5,5mm TroQ Trocar Spikes, Olympus Winter & Ibe GmbH PDF, 90KB, File does not meet accessibility standards Date: 28. May 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01467/10

Corrective Action for HeartStart MRx, Philips PDF, 163KB, File does not meet accessibility standards Date: 28. May 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01738/10

Safety Notice for NexGen Complete Knee Solution MIS Tibial Component, Zimmer Inc. PDF, 53KB, File does not meet accessibility standards Date: 28. May 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01740/10

Recall for Flexima Biliary Stent Systems, Boston Scientific PDF, 64KB, File does not meet accessibility standards Date: 28. May 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01788/10

Lot Recall for LARGE QWIX screws, Newdeal PDF, 82KB, File does not meet accessibility standards Date: 27. May 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01418/10

Urgent Safety Notice on implantable cardioverter defibrillators Convert+ V-195, St. Jude Medical PDF, 126KB, File does not meet accessibility standards Date: 27. May 2010 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01797/10

Safety Notice for Consulta CRT-D, Secura DR/VR, Concerto II CRT-D, Virtuoso II DR/VR, Maximo II CRT-D und Maximo II DR/VR, Medtronic PDF, 17KB, File does not meet accessibility standards Date: 27. May 2010 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01808/10