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Corrective action of the HeartStart MRx Monitor/Defibrillator, Philips Healthcare PDF, 51KB, File does not meet accessibility standards Date: 09. July 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 03632/13

Recall for Uric Acid AOX, Thermo Fisher PDF, 187KB, File does not meet accessibility standards Date: 08. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06800/12

Corrective action for Advia Centaur Systems, Dimension Systems, Dimension Vista Systems und Immulite Systems, Siemens PDF, 42KB, File does not meet accessibility standards Date: 08. July 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03015/13

Recall for the Neuroform 3™ Microdelivery Stent System, Boston Scientific PDF, 94KB, File does not meet accessibility standards Date: 08. July 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 03483/13

Updated Safety Notice for GemStarInfusion System, Hospira Inc. PDF, 725KB, File does not meet accessibility standards Date: 08. July 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01263/13

Recall of the Reduction Instrument for Spondylolisthesis standard, Synthes GmbH PDF, 527KB, File does not meet accessibility standards Date: 08. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03595/13

Lot Recall of tangoRS Rods, ulrich GmbH PDF, 14KB, File does not meet accessibility standards Date: 08. July 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03602/13

Recall for the MedStream® Programmable Infusion System, Codman Neuro Sciences PDF, 118KB, File does not meet accessibility standards Date: 08. July 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - drug pumps
Reference 03298/13

Corrective Action for Licox CMP Catheter Kits, GMS PDF, 101KB, File does not meet accessibility standards Date: 05. July 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03447/13

Recall for the Oxford Fixed Lateral Bearings, Biomet PDF, 39KB, File does not meet accessibility standards Date: 04. July 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02728/13

Recall for the Dynamic Locking Screw Stardrive®, SYNTHES PDF, 478KB, File does not meet accessibility standards Date: 04. July 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03419/13

Recall for the EverFlex™ Vascular Stent System, ev3 Incorporated PDF, 142KB, File is accessible Date: 04. July 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 03360/13

Corrective action for Thermo Scientific QMS Teicoplanin Reagent, Microgenics PDF, 444KB, File does not meet accessibility standards Date: 04. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03619/13

Lot Recall for KIMGUARD* Container Filters, Kimberly-Clark PDF, 128KB, File does not meet accessibility standards Date: 04. July 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 01840/13

Corrective action for CoaguChek XS analysers, CoaguChek XS Plus analysers and CoaguChek XS Pro analysers, Roche PDF, 120KB, File does not meet accessibility standards Date: 03. July 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02707/13

Lot Recall of the laser fibre of model line SLT, PhotoMedex PDF, 176KB, File does not meet accessibility standards Date: 03. July 2013 Type: Customer information

Product group Optics / Precision engineering - laser technology
Reference 02544/13

Safety Notice for the STAR Excimer Laser System, AMO Ireland PDF, 584KB, File does not meet accessibility standards Date: 03. July 2013 Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 03256/13

Recall of the medical device monopolar electrodes, Bissinger PDF, 364KB, File does not meet accessibility standards Date: 03. July 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02584/13

Corrective Action regarding the aura6000-THN sleep therapy system, ImThera Medical Inc. PDF, 21KB, File does not meet accessibility standards Date: 03. July 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 02814/13

Corrective action for BBL™ Crystal™ Enteric Nonfermenter ID Kit, BD PDF, 669KB, File does not meet accessibility standards Date: 03. July 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00765/13

Corrective action for Antimicrobial Susceptibility Testing Discs CN10, Oxoid PDF, 17KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 02751/13

Safety Notice for the Belmont®Rapid Infuser, Belmont PDF, 240KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 03388/13

Safety Notice for the VenaFlow 30B-B and 30 BI-B, DJO Global PDF, 57KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Physical therapy - massage / mobility devices
Reference 03260/13

Safety Notice for the Liko® Overhead and Mobile Lifts - Standard SlingBar™ 450, Hill-Rom Company PDF, 833KB, File does not meet accessibility standards Date: 02. July 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 02783/13

Lot Recall of the Guide Wire Ø 2.5 mm with drill tip, lenghts 300 mm, DePuy Synthes PDF, 747KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02676/13

Safety Notice concerning the reusable CO2 absorbent canister, GE Healthcare PDF, 174KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03259/13

Recall for the BD Plastipak 50 ml Luer Lok Syringe, Becton Dickinson PDF, 48KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 03531/13

Recall for the 1L Receptal Systems (Liners and Canisters), Hospira PDF, 447KB, File does not meet accessibility standards Date: 01. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01916/13

Corrective action for Seraclone Anti-S, Biotest PDF, 601KB, File does not meet accessibility standards Date: 01. July 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 01899/13

Safety Notice concerning the Patient Transporter TRANSLIFE 4749.01A0, Maquet GmbH PDF, 206KB, File does not meet accessibility standards Date: 01. July 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 02355/13