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Recall of the Ammonium reagent from Bayer PDF, 40KB, File does not meet accessibility standards Date: 01. March 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00300/07

Corrective action and recall of the Benzodiazepin reagent from Bayer PDF, 48KB, File does not meet accessibility standards Date: 01. March 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00299/07

Recall of the dual chamber C- and T-series pacemakers from Vitatron PDF, 76KB, File does not meet accessibility standards Date: 01. March 2007 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00310/07

Information for the Flexor Check-Flo Micropuncture Introducer Sets from William Cook PDF, 69KB, File does not meet accessibility standards Date: 01. March 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03740/06

Recall of the BD Procount Kit with lot number 65857 from Becton Dickinson PDF, 39KB, File does not meet accessibility standards Date: 16. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00344/07

Recall of the Architect LH reagent from Abbott PDF, 58KB, File does not meet accessibility standards Date: 16. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03533/06

Recall of TriGen InterTan from Smith & Nephew PDF, 53KB, File does not meet accessibility standards Date: 14. February 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00397/07

Recall of the Slidex Meningitis Kit 5 from BioMérieux PDF, 90KB, File does not meet accessibility standards Date: 14. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00012/07

Recall of the lot number SC058 of Capture-R Select from Immucor PDF, 50KB, File does not meet accessibility standards Date: 13. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03798/06

Recall of Colorado 2 Anterior Plates from Medtronic PDF, 73KB, File does not meet accessibility standards Date: 13. February 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00392/07

Information concerning the Infinity Docking Stations from Dräger PDF, 79KB, File does not meet accessibility standards Date: 09. February 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00005/07

Recall of the lot number A06J02257 of the Amicus Apheresis Set (R4R2340) from Baxter PDF, 60KB, File does not meet accessibility standards Date: 09. February 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00371/07

Recall of the Guardian™ Hemostasis Valves from Zerusa PDF, 72KB, File does not meet accessibility standards Date: 08. February 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00360/07

Recall of the Rocker Reducer Instrument from Medtronics PDF, 44KB, File does not meet accessibility standards Date: 07. February 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03647/06

Recall of the Quantum Biliary Dilation Catheter from Cook Endoscopy PDF, 39KB, File does not meet accessibility standards Date: 06. February 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00342/07

Recall of the Air Optix (O2 Optix) soft contact lenses from CIBA Vision PDF, 149KB, File does not meet accessibility standards Date: 06. February 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 00142/07

Recall of Safe Cut Biopsy Systems from Somatex PDF, 74KB, File does not meet accessibility standards Date: 06. February 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03788/06

Important Safety Notices concerning the Pari inhalers from Pari PDF, 61KB, File does not meet accessibility standards Date: 06. February 2007 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 02906/06

Information concerning the operating tables from Trumpf PDF, 311KB, File does not meet accessibility standards Date: 06. February 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03813/06

Software error in the Schwind CAM software from Schwind eye-tech-solutions PDF, 86KB, File does not meet accessibility standards Date: 02. February 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03687/06

Safety information for the wheelchair model 1.300 UF from Uniroll PDF, 118KB, File does not meet accessibility standards Date: 02. February 2007 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03781/06

Corrective action of the cards for susceptibility testing for the analyzers Vitek, Vitek 2 and Vitek compact from bioMèrieux PDF, 96KB, File does not meet accessibility standards Date: 02. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00339/07

Corrective action of the Vitek GPS-531, Vitek GPS-532 and Vitek GPS-533 cards for susceptibility testing from bioMèrieux PDF, 55KB, File does not meet accessibility standards Date: 02. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00318/07

Corrective action and recall of the Sample Management System (software version 2.2) from DPC Biermann PDF, 84KB, File does not meet accessibility standards Date: 01. February 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00261/07

Software update for the Telemetrie-Systems ApexPro/ApexPro CH from GE Healthcare PDF, 73KB, File does not meet accessibility standards Date: 01. February 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03795/06

Recall of ConMed Linvatec Ultra Power Burs and ConMed Linvatec E9000 Burs PDF, 776KB, File does not meet accessibility standards Date: 01. February 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03746/06

Recall of the Syva Emit 2000 Phenobarbital test from Dade Behring PDF, 39KB, File does not meet accessibility standards Date: 30. January 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00194/07

Corrective action concerning the Integris and Allura Xper X‑Ray Systems from Philips PDF, 70KB, File does not meet accessibility standards Date: 30. January 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00269/07

Corrective action of the clinical chemistry system Dimension RxL Max with STM from Dade Behring PDF, 26KB, File does not meet accessibility standards Date: 30. January 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00193/07