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Recall for OtisMed ShapeMatch Cutting Guides, Stryker PDF, 767KB, File does not meet accessibility standards Date: 27. November 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02082/13

Recall for FreeStyle Lite® test strips, Abbott PDF, 85KB, File does not meet accessibility standards Date: 27. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06883/13

Lot Recall for FMS Duo+ and FMS Solo surgical irrigation tubing sets, DePuy Synthes PDF, 685KB, File does not meet accessibility standards Date: 27. November 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05220/13

Corrective action for HemosIL AcuStar HIT-Ab(PF4-H), Instrumentation Laboratory PDF, 32KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05493/13

Corrective action for chromID Salmonella Agar, bioMérieux PDF, 219KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05424/13

Safety Notice for the Ingenuity TF PET/CT Software Version 4.0, Philips Healthcare PDF, 234KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 05414/13

Recall for the VariAx Compression Plates, STRYKER PDF, 539KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05875/13

Safety Notice for the Helical Blade for TFN, SYNTHES PDF, 3MB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05943/13

Safety Notice for Central Monitor CNS-6201 series, Nihon Kohden PDF, 204KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06846/13

Recall of the Magstim 90mm High Power Coil, Magstim Company Limited PDF, 62KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05584/13

Urgent Safety Notice for the Application Instrument for Sternal ZipFix™, Synthes GmbH PDF, 73KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05283/13

Corrective action for Advia 1200, 1650, 1800 and 2400 Chemistry Systems, Siemens PDF, 26KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05355/13

Lot Recall of VORTEK® Double Loop Ureteral Stent Open/Open With Connectable Pusher and VORTEK® Hydro-Coated Double Loop Ureteral Stents, Coloplast PDF, 66KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 04072/13

Recall of several dental implants, Biomet 3i PDF, 105KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 05349/13

Urgent Safety Notice for the ADM®/MDM® Ball Impactor Tip and ADM® RIM Impactor Tip Instruments, Stryker PDF, 97KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06067/13

Recall of BellaTek Zirconia-Abutments, BIOMET 3i PDF, 71KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 05318/13

Recall of Pediatric Arterial Cannula, Maquet PDF, 678KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05451/13

Safety Notice concerning several models of SlingBars, Liko GmbH PDF, 368KB, File does not meet accessibility standards Date: 22. November 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 06050/13

Safety Notice for Argyle™ Single Lumen Polyurethane Umbilical Vessel Catheters, Covidien PDF, 20KB, File does not meet accessibility standards Date: 22. November 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05465/13

Urgent Safety Notice about the stop of using all Neptune Waste Management Systems in Germany, Stryker PDF, 75KB, File does not meet accessibility standards Date: 22. November 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03476/12

Urgent Safety Notice for the optimys® Opening Broach bent, Mathys AG PDF, 130KB, File does not meet accessibility standards Date: 22. November 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05718/13

Complete Recall of all Lenscare SH-System monthly contact lenses, 4CARE GmbH PDF, 16KB, File does not meet accessibility standards Date: 22. November 2013 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - contact lenses
Reference 06785/13

Lot Recall of the Original- Perfusor® Syringe 50 ml without cannula, B.Braun PDF, 38KB, File does not meet accessibility standards Date: 22. November 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 06946/13

Lot Recall of the Vector TAS Screws, ORMCO PDF, 189KB, File does not meet accessibility standards Date: 21. November 2013 Topics: Medical devices Type: Customer information

Product group Dental products - orthodontic equipment
Reference 04477/13

Safety Notice for the Epilor Loss of Resistance Syringe, Becton Dickinson PDF, 106KB, File does not meet accessibility standards Date: 21. November 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 05164/13

Urgent Safety Notice concerning the disposable breathing circuit Ref. Nr. 270.743, WILAmed PDF, 712KB, File does not meet accessibility standards Date: 21. November 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03316/13

Safety Notice for the device Glandomed Medizinische Mundspüllösung, CELL PHARM PDF, 34KB, File does not meet accessibility standards Date: 21. November 2013 Topics: Medical devices Type: Customer information

Product group Dental products - others
Reference 00684/13

Lot Recall for Intrafix Primeline / Intrafix Air P sets, B. Braun Melsungen AG PDF, 44KB, File does not meet accessibility standards Date: 21. November 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion kits
Reference 06461/13

Corrective action for the cobas HbA1c Test on the cobas b101 System, Roche PDF, 99KB, File does not meet accessibility standards Date: 21. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05375/13

Urgent Safety Notice concerning the material of tubing in dosage pump of miniETD2 PAA and Maintenance kits of miniETD2 PAA / ETD3 PAA, Olympus PDF, 3MB, File does not meet accessibility standards Date: 21. November 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 06451/13