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Recall for Tibia Offset Stem of the ENDURO / COLUMBUS REVISION Knee System, Aesculap PDF, 49KB, File is accessible Date: 10. August 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02690/10

Recall of Nephrostomy Sets, Urotech GmbH PDF, 349KB, File is accessible Date: 10. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01741/10

Safety Notice concerning Online Substitution Line for Dialog, B. Braun Avitum PDF, 142KB, File is accessible Date: 10. August 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01925/10

Safety Notice for BD HPMC Solution, Becton Dickinson PDF, 57KB, File is accessible Date: 10. August 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01999/10

Safety Notice for Skippi power wheelchair for children, Otto Bock PDF, 166KB, File is accessible Date: 09. August 2010 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02465/10

Safety Notice for Forefoot Cannulated Drill Sterile, Newdeal PDF, 574KB, File is accessible Date: 09. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02558/10

Recall for Antireflux Valve Ureteral Stent Sets for Children, Teleflex Medical PDF, 143KB, File is accessible Date: 09. August 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02052/10

Safety Notice for Rückenmaschine med, Milon Industries PDF, 45KB, File is accessible Date: 09. August 2010 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 02269/10

Safety Notice about HMRS Anchorage Stems, Stryker PDF, 145KB, File is accessible Date: 09. August 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01488/10

Recall of FemSoft® urethral inserts, Rochester Medical PDF, 131KB, File is accessible Date: 09. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01910/10

Safety Notice for PEGA® TUBE, Venner Medical (Deutschland) GmbH PDF, 63KB, File is accessible Date: 06. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00373/10

Recall for GlucoHEXAL ® II strips, Medwatch GmbH PDF, 121KB, File is accessible Date: 06. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02180/10

Recall for HemoStat Thromboplastin-SI, Human PDF, 78KB, File is accessible Date: 06. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02054/10

Safety Information for angle-stable distal femoral plates, KÖNIGSEE IMPLANTATE PDF, 2MB, File is accessible Date: 06. August 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01134/10

Safety Notice for radiotherapy treatment planning software iPlan RT dose, BrainLab PDF, 125KB, File is accessible Date: 06. August 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01192/10

Lot Recall for Elect balloon catheter, Biotronic PDF, 65KB, File is accessible Date: 06. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02047/10

Lot Recall for ProTack fixation device, Covidien PDF, 69KB, File is accessible Date: 06. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02291/10

Recall of ABC Screwdriver F/Selflocking Screws, Art. No. FJ910R with UNICOS cording C100A to C100U, Aesculap AG PDF, 76KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02495/10

Lot recall of NQ527-Columbus CR/PS Trial Gl.Surf. T2/2+ 14mm in Columbus Set Basic Tibia Trial Implant (NQ404), Aesculap AG PDF, 174KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02206/10

Safety Notice for directCheck Whole Blood Control, International Technidyne Corp. PDF, 117KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01981/10

Safety Notice for Panther Radiation Treatment Planning System, Prowess Inc. PDF, 240KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02399/10

Safety Notice for Paraffine Heater PT15, Heuser Apparatebau PDF, 123KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 02415/10

Lot recall of dental adhesive Futurabond NR, VOCO PDF, 90KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 01914/10

Recall for SpineJack Preparation Kit, Vexim SAS PDF, 95KB, File is accessible Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02456/10

Recall of Syncro-14 und Syncro² Guidewires PDF, 75KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02155/10

Recall of certain lots of BARD® DORADO® PTA Dilatation Catheters, Bard Peripheral Vascular Inc. PDF, 47KB, File is accessible Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01927/10

Safety Notice for exudates collection pouches (1000 ml, Ref 25294) with Suprasorb CNP P1, Lohmann & Rauscher GmbH & Co. KG PDF, 23KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02100/10

Lot Recall for PSD Gel packed with different Peri-Strips devices, Synovis Surgical Innovations PDF, 43KB, File is accessible Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02476/10

Lot Recall for ReNu® Multi-Purpose Solution and ReNu® MultiPlus Solution, Bausch + Lomb PDF, 80KB, File does not meet accessibility standards Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02389/10

Lot Recall for Heartstring Aortic Cutter 4,3 mm, Maquet PDF, 98KB, File is accessible Date: 05. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02216/10