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14,984 results

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Lot Recall of the suture Safil Quick, B. Braun Surgical PDF, 374KB, File does not meet accessibility standards Date: 20. June 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 03033/13

Lot Recall of LINO and DILENE surgical sutures, B. Braun Surgical PDF, 800KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 01878/13

Recall of Parallel Walled Implants, BIOMET 3i PDF, 20KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 02796/13

Safety Notice for the hospital bed Evolution™ LI156, Hill Rom PDF, 23KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 07421/12

Urgent Safety Notice regarding implantable HeartWare® VAS, HeartWare Inc. PDF, 136KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 03243/13

Urgent Safety Notice for Consulta® CRT-P and Syncra® CRT-P devices, Medtronic PDF, 29KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - cardiac pacemakers
Reference 03240/13

Expanded Safety Notice for the product Berman Angiography catheter, Arrow International PDF, 145KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00056/13

Recall of Lead Cups used for capping of implantable Deep Brain Stimulation Leads (DBS), Medtronic PDF, 150KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 00665/13

Safety Notice concerning Optima C-10 Probetester, Külzer Medizintechnik PDF, 239KB, File does not meet accessibility standards Date: 17. June 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 05292/12

Incorrect heart rate value on Aloka Prosound F75, Hitachi PDF, 246KB, File does not meet accessibility standards Date: 12. June 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02873/13

Lot recall of professional tooth whitening device Home Whitening, WHITEsmile PDF, 188KB, File does not meet accessibility standards Date: 12. June 2013 Topics: Medical devices Type: Customer information

Product group Dental products - others
Reference 02869/13

Safety Notice for the hospital bed HR900A, Hill Rom PDF, 90KB, File does not meet accessibility standards Date: 11. June 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 01288/13

Safety Notice for the sterilizer typ S, Memmert PDF, 612KB, File does not meet accessibility standards Date: 11. June 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 02320/13

Lot Recall of the GelPOINT Advanced Access Platform, Applied Medical PDF, 91KB, File does not meet accessibility standards Date: 11. June 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 02444/13

Lot Recall for the Bracket Buccal Tubes, ORMCO PDF, 156KB, File does not meet accessibility standards Date: 10. June 2013 Topics: Medical devices Type: Customer information

Product group Dental products - orthodontic equipment
Reference 01884/13

Safety Notice for the GE Extremity 1.5T MR Scanners (Optima MR 430s / MSK 1.5 Tesla Extreme), GE Healthcare PDF, 69KB, File does not meet accessibility standards Date: 06. June 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 01656/13

Lot Recall of the product Procera abutment Ti for Astra Tech 4,5/5,0 ST, Nobel Biocare AB PDF, 28KB, File does not meet accessibility standards Date: 03. June 2013 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02300/13

Recall of two lots of Pasteur Pipets for in-vitro-fertilisation, Origio Inc. PDF, 18KB, File does not meet accessibility standards Date: 29. May 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - dosing systems
Reference 02286/13

Urgent Safety Notice for the STERRAD® CYCLESURE® 24 Biological Indicators, ASP (Johnson & Johnson MEDICAL GmbH) PDF, 102KB, File does not meet accessibility standards Date: 23. May 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 02459/13

Corrective action for Elecsys b-CrossLaps, Roche PDF, 98KB, File does not meet accessibility standards Date: 22. May 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 02400/13

Problem with STERRAD® 100NX® and STERRAD® 200 Sterilization Systems, ASP (Advanced Sterilization Products) PDF, 23KB, File does not meet accessibility standards Date: 22. May 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 01750/13

Lot recall of dental filling material x-tra fil caps, VOCO PDF, 139KB, File does not meet accessibility standards Date: 16. May 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 01904/13

Recall of several vaginal pessaries intended for prolapse uteri or incontinence, Cooper Surgical PDF, 232KB, File does not meet accessibility standards Date: 15. May 2013 Topics: Medical devices Type: Customer information

Product group Contraception - intrauterine device
Reference 01389/13

Lot recall of Milex™ Wide-Seal contraceptive vaginal silicone diaphragm, Cooper Surgical PDF, 197KB, File does not meet accessibility standards Date: 15. May 2013 Topics: Medical devices Type: Customer information

Product group Contraception - diaphragms
Reference 01388/13

Safety Notice for the product VersaCut Morcellator, Lumenis PDF, 236KB, File does not meet accessibility standards Date: 10. May 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07935/12

Expanded Recall concerning Vitrea Z-Axis Measurement Error on Vitrea software versions, Vital Images PDF, 181KB, File does not meet accessibility standards Date: 10. May 2013 Topics: Medical devices Type: Customer information

Product group Medical data processing (software) - software for diagnostic radiology
Reference 00658/13

Safety Notice for the BariAir™ Therapy System, ArjoHuntleigh PDF, 50KB, File does not meet accessibility standards Date: 07. May 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 02482/13

Recall for the product ProcedurePak®, Mölnlycke Healthcare PDF, 24KB, File does not meet accessibility standards Date: 06. May 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 02440/13

Safety Notice for XVI R3.5, R4.0, R4.2, and R4.5, Elekta PDF, 193KB, File does not meet accessibility standards Date: 06. May 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00317/13