BfArM - Federal Institute for Drugs and Medical Devices

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15,004 results

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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