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Corrective Action of Siemens Healthcare Diagnostics Inc. for calibrators PDF, 46KB, File does not meet accessibility standards Date: 07. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04040/08

Recall of the adaptor Combifix from the manufacturer B.Braun Melsungen AG PDF, 2MB, File does not meet accessibility standards Date: 07. November 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03748/08

Recall of certain lots of PE biliary stents of the manufacturer Dispomedica GmbH PDF, 697KB, File does not meet accessibility standards Date: 07. November 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03666/08

Recall of the products Tetrisal S nose drops PDF, 74KB, File does not meet accessibility standards Date: 07. November 2008 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 02367/08

Recall of blood bag systems named Composelect of manufacturer Fresenius Kabi GmbH PDF, 102KB, File does not meet accessibility standards Date: 07. November 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04027/08

Recall of femoral heads from Stryker Orthopaedics PDF, 2MB, File does not meet accessibility standards Date: 06. November 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04179/07

Corrective action / Recall of Beckman Coulter for Access Immunoassay Systems Assay Protocol File Software PDF, 115KB, File does not meet accessibility standards Date: 06. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03989/08

Field Safety Notice about CT syngo Dual Energy Viewer from Siemens Healthcare PDF, 967KB, File does not meet accessibility standards Date: 06. November 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03586/08

Field Safety Notice with Elekta® MLC Software PDF, 37KB, File does not meet accessibility standards Date: 06. November 2008 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02313/08

Field Safety Notice for Pegasus 3-D-System from Biofeedback Motor Control GmbH PDF, 25KB, File does not meet accessibility standards Date: 06. November 2008 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 03661/08

Safety Notice with iSite PACS from Philips Healthcare PDF, 203KB, File does not meet accessibility standards Date: 05. November 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03999/08

Information from Edwards Lifesciences of Vigilance II Monitors PDF, 2MB, File does not meet accessibility standards Date: 05. November 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03850/08

Further Corrective Actions concerning Pari inhalers PDF, 441KB, File does not meet accessibility standards Date: 05. November 2008 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 00700/08

Recall from K-Flow Access Catheters PDF, 82KB, File does not meet accessibility standards Date: 05. November 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03698/08

Urgent Field Safety Notice regarding the 2490C CareLink Monitor software from Medtronic. PDF, 14KB, File does not meet accessibility standards Date: 05. November 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03930/08

Smiths Medical Int. Ltd. Recalls another lot of the Portex Blue Line Ultra Tracheostomy Sets PDF, 49KB, File does not meet accessibility standards Date: 05. November 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03927/08

Recall of Stephany Diagnostika for Secu-Troponin I PDF, 93KB, File does not meet accessibility standards Date: 05. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03467/08

Tryton Side Branch Stent: The company Tryton Medical has informed about a lot recall of these products PDF, 39KB, File does not meet accessibility standards Date: 04. November 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03914/08

The company Haag-Streit AG notified customers of a possible leaking of tonometer prisms PDF, 880KB, File does not meet accessibility standards Date: 04. November 2008 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03184/08

Corrective Action of Siemens Healthcare Diagnostics Inc. for Assayed Chemistry Controls 1 and 2 of ADVIA Chemistry Systems PDF, 57KB, File does not meet accessibility standards Date: 03. November 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03918/08

Recall for Safety-Lancet, Sarstedt PDF, 39KB, File does not meet accessibility standards Date: 30. October 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03313/08

Recall for DePuy G2® cementless hipstem, DePuy PDF, 202KB, File does not meet accessibility standards Date: 30. October 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03898/08

Recall for Drill handle, Straumann AG PDF, 39KB, File does not meet accessibility standards Date: 30. October 2008 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 03979/08

Recall/Corrective action for ADVIA Centaur CP, Siemens PDF, 82KB, File does not meet accessibility standards Date: 30. October 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03882/08

Recall for Gravity Compensating Accessory, Integra Neurosciences PDF, 104KB, File does not meet accessibility standards Date: 29. October 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03889/08

Recall for Fem-Flex Femoral Arterial Cannulae, Edwards PDF, 104KB, File does not meet accessibility standards Date: 29. October 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03975/08

Recall for VCare uterine manipulators, ConMed PDF, 113KB, File does not meet accessibility standards Date: 29. October 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03333/08

Recall for BD Anaesthesia Kits and Epidural Filter, Becton Dickinson PDF, 175KB, File does not meet accessibility standards Date: 24. October 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03844/08

Information for Colleague Triple Channel Pumps, Baxter PDF, 74KB, File does not meet accessibility standards Date: 24. October 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03643/07