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Recall of the iMRI Registration Matrix for GE Headholder of the Cranial Navigation System, Brainlab AG PDF, 139KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02898/13

Recall for VITROS Chemistry Products PHBR Slides, Ortho Clinical Diagnostics PDF, 177KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01425/13

Safety Notice for the Image Diagnost (IDI) Collaboration Server, GE Healthcare PDF, 44KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group Radiological technology - radiological equipment for mammographic diagnostics
Reference 01646/13

Important Safety Informations concerning intracardiac catheter measuring stations of the Schwarzer “evo” series, Schwarzer GmbH PDF, 185KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 02309/13

Lot Recall of the Versaport ™ Bladeless Optical 5mm Trocar with Fixation Cannula, Covidien PDF, 54KB, File does not meet accessibility standards Date: 03. June 2013 Type: Customer information

Product group Medical instruments for use in humans - visceral surgery
Reference 02749/13

Lot Recall for the CMF MatrixMidface, Mandible, Orthognatic Screws and CMF MatrixNeuro Screws, SYNTHES PDF, 2MB, File does not meet accessibility standards Date: 03. June 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02313/13

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

Safety Notice for Brilliance 64, Ingenuity, Ingenuity Core and Ingenuity Core128 CT systems, Philips Healthcare PDF, 373KB, File does not meet accessibility standards Date: 03. June 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 02162/13

Lot Recall of procedure packs, M.E.D. Medical Products GmbH PDF, 35KB, File does not meet accessibility standards Date: 03. June 2013 Type: Customer information

Product group ophthalmological technology - other medical devices for ophthalmological purposes
Reference 01965/13

Lot Recall for the Medi-Trace™ Cadence Adult and Pediatric Radiotransparent Defibrillation Electrodes, Covidien PDF, 20KB, File does not meet accessibility standards Date: 03. June 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02203/13

Safety Notice concerning the automated Blood Collection System Trima Accel, Terumo BCT PDF, 377KB, File does not meet accessibility standards Date: 01. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 02797/13

Lot Recall of the Burr Attachments M and L, DePuy Synthes PDF, 369KB, File does not meet accessibility standards Date: 31. May 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02633/13

Safety Notice concerning a software update for the control console of the Digital Linear Accelerator, Siemens Healthcare PDF, 26KB, File does not meet accessibility standards Date: 31. May 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 02753/13

Urgent Safety Notice for the Edwards Lifesciences Crimper for Transcatheter Heart Valve systems PDF, 28KB, File does not meet accessibility standards Date: 31. May 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01755/13

Safety Notice for the DANA Diabecare R Insulin Pumps, Sooil Development PDF, 595KB, File does not meet accessibility standards Date: 31. May 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 00718/13

Rückruf diverser Lose des Collins Radioparent Sternal Blade, Symmetry Surgical PDF, 661KB, File does not meet accessibility standards Date: 31. May 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02417/13

Safety Notice for the product Digital Accelerator / Integrity™ 1.1., Elekta PDF, 144KB, File does not meet accessibility standards Date: 31. May 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 02032/13

Recall for BBL™ DrySlide™ PYR Kit and BBL™ DrySlide™ Oxidase Kit, Becton Dickinson PDF, 44KB, File does not meet accessibility standards Date: 31. May 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 02157/13

Corrective action for Cobas Ampliprep, Roche PDF, 101KB, File does not meet accessibility standards Date: 31. May 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 06315/12

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

Lot Recall for the VascuTape® (Glow ’N Tell® Tape, LeMaitre® Stent Guide), LeMaitre Vascular GmbH PDF, 55KB, File does not meet accessibility standards Date: 29. May 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 01600/13

Recall for LINEZOLID 0.4mg ADATAB, Mast Diagnostica PDF, 395KB, File does not meet accessibility standards Date: 29. May 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01104/13

Recall for epoc BGEM-Test Card, Epocal PDF, 40KB, File does not meet accessibility standards Date: 29. May 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01792/13

Synthes: Recall of all lots of the Soft Tissue Retractor, small, extendible. PDF, 372KB, File does not meet accessibility standards Date: 28. May 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02668/13

Recall for Access Immunoassay Systems Vitamin B12 Reagent Kit, Beckman Coulter PDF, 59KB, File does not meet accessibility standards Date: 28. May 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01799/13

Recall for Remel StreptexGroup D Latex Reagent, Oxoid PDF, 19KB, File does not meet accessibility standards Date: 28. May 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01992/13

Recall of the Integra Ojemann Cortical Stimulator OCS2, Integra LifeSciences Services PDF, 316KB, File does not meet accessibility standards Date: 28. May 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02023/13

Safety Notice for the OPTEASE® Retrievable Vena Cava Filter, Cordis PDF, 258KB, File does not meet accessibility standards Date: 28. May 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 02168/13

Recall for one lot of the Glenosphere Orientation Guide Instrument, DePuy France SA PDF, 201KB, File does not meet accessibility standards Date: 27. May 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02831/13