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14,972 results

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Recall for Covidien Devon™ Light Gloves and certain sub-assembly kits that include the Devon™ Light Gloves, Covidien LLC PDF, 158KB, File does not meet accessibility standards Date: 21. May 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02477/15

Corrective action for the toilet raiser fixed Hi-Loo and toilet armrest Supporter, Etac Supply Center AB PDF, 500KB, File does not meet accessibility standards Date: 21. May 2015 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - daily living aids
Reference 02439/15

Safety Notice/Recall for the product "Lampengriffbezüge", Fuhrmann GmbH PDF, 101KB, File does not meet accessibility standards Date: 20. May 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03070/15

Urgent Safety Notice for Covidien Devon™ Light Glove in KitPack® OP-Setsystems, Lohmann & Rauscher GmbH & Co. KG PDF, 29KB, File does not meet accessibility standards Date: 20. May 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02602/15

Safety Notice/Recommendations for the safe use of the Catalys® Precision Laser System, Optimedica Corporation PDF, 114KB, File does not meet accessibility standards Date: 20. May 2015 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 03067/15

Recall for Covidien Devon™ Light Gloves (also included in certain sub-assembly kits), Medtronic/Covidien PDF, 235KB, File does not meet accessibility standards Date: 20. May 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02850/15

Corrective action for the Getinge 86-series washer-disinfectors, Getinge Disinfection AB PDF, 3MB, File does not meet accessibility standards Date: 19. May 2015 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 03011/15

Recall for the Chisel Blade, Synthes GmbH PDF, 3MB, File does not meet accessibility standards Date: 19. May 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03008/15

Safety Notice for the Philips DigitalDiagnost 4.0.x, Philips Medical Systems PDF, 2MB, File does not meet accessibility standards Date: 19. May 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 02944/15

Corrective action for the Dimension Vista® Phenytoin Flex® reagent cartridge, Siemens Healthcare Diagnostics PDF, 24KB, File does not meet accessibility standards Date: 19. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02415/15

Safety Notice for the product Ki67-MM1, Leica Biosystems PDF, 2MB, File does not meet accessibility standards Date: 19. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 02312/15

Urgent Safety Notice for the product D-Dimer Gen.2, Roche Diagnostics PDF, 103KB, File does not meet accessibility standards Date: 19. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02420/15

Safety Information for the RELIANCE 4-FRONT single coil defibrillation leads, Boston Scientific Corporation PDF, 230KB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 03051/15

Recall for the product Dermaroller MC, Dermaroller GmbH PDF, 3MB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - auxiliary equipment
Reference 02995/15

Corrective action for the HeartAttendant Interface Cable, ReliantHeart Inc. PDF, 31KB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 03037/15

Corrective action for the VenaSeal™ Closure System, Covidien Deutschland GmbH PDF, 152KB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 02675/15

Corrective action for the Philips Ultrasound EPIQ 7 Ultrasound System, Philips Healthcare - Ultrasound PDF, 292KB, File does not meet accessibility standards Date: 18. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02875/15

Recall for DAT IgG-Dilution ID-Card, BioRad/DiaMed GmbH PDF, 1MB, File does not meet accessibility standards Date: 12. May 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 02535/15

Safety Information for the product minisart (Exchange of mislabeled packages from lot 50057103), Sartorius Stedim Biotech GmbH PDF, 2MB, File does not meet accessibility standards Date: 12. May 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - filters
Reference 02001/15

Follow-up Information for the Animas® 2020 and IR 1200 Insulin Pumps, Animas Corporation PDF, 128KB, File does not meet accessibility standards Date: 12. May 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 06616/12

Batch Recall for the Infusomat Space Line UV-Protect, B. Braun Melsungen AG PDF, 36KB, File does not meet accessibility standards Date: 12. May 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 02724/15

Corrective action for the Philips Model AFFINITI 70 Ultrasound System, Philips Healthcare Ultrasound PDF, 224KB, File does not meet accessibility standards Date: 12. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02866/15

Important Information for the Accu-Chek® Spirit Combo insulin pump, Roche Diagnostics PDF, 132KB, File does not meet accessibility standards Date: 12. May 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 02218/15

Urgent Safety Notice for the power cords of the respiratory therapy devices Trend II, point und Vector et., Hoffrichter GmbH PDF, 433KB, File does not meet accessibility standards Date: 11. May 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01412/15

Safety Notice for the Philips Model AFFINITI 50 Ultrasound System, Philips Healthcare Ultrasound PDF, 189KB, File does not meet accessibility standards Date: 11. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02891/15

Corrective action for the Galaxy Unyco Diaphyseal tibia sterile kit, Orthofix Srl PDF, 138KB, File does not meet accessibility standards Date: 11. May 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02684/15

Urgent Safety Notice/Corrective action for Terumo® Radifocus Guide Wire M, Terumo Europe NV PDF, 104KB, File does not meet accessibility standards Date: 11. May 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02814/15

Urgent Safety Notice for the Philips EPIQ 5 Ultrasound System, Philips Healthcare Ultrasound PDF, 323KB, File does not meet accessibility standards Date: 11. May 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02892/15

Updated Information for the 3f Enable™ Aortic Bioprosthesis (Model 6000), Medtronic PDF, 93KB, File does not meet accessibility standards Date: 11. May 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 07774/14