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14,972 results

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Urgent Safety Notice for the OPTIMEDICA Catalys® Precision Laser System, OptiMedica Corporation PDF, 113KB, File does not meet accessibility standards Date: 30. June 2015 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 03068/15

Corrective action for the Acetaminophen assay, Sekisui Diagnostics P.E.I. Inc. PDF, 160KB, File does not meet accessibility standards Date: 30. June 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02965/15

Urgent Safety Notice – Easypump II Recall, B. Braun Melsungen AG PDF, 68KB, File does not meet accessibility standards Date: 30. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 04091/15

Urgent Safety Notice for the CADD®-Solis Ambulatory Infusion Pumps, Smiths Medical ASD PDF, 171KB, File does not meet accessibility standards Date: 30. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 03334/15

Corrective action for the PROCISE EZ View™ with Integrated Cable and EVAC™ 70 XTRA with Integrated Cable Wands, Smith & Nephew PDF, 70KB, File does not meet accessibility standards Date: 30. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 03711/15

Corrective action for the multiFiltratePRO devices, Fresenius Medical Care PDF, 40KB, File does not meet accessibility standards Date: 30. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 03915/15

Recall for the SofPort & SoFlex intraocular lenses, Bausch + Lomb PDF, 48KB, File does not meet accessibility standards Date: 30. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03560/15

Urgent Safety Notice for the product RayStation, RaySearch Laboratories PDF, 486KB, File does not meet accessibility standards Date: 29. June 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 03159/15

Urgent Safety Notice for the ATTUNE® INTUITION™ Tibial Articulation Surface Instruments, DePuy Orthopaedics, Inc. PDF, 703KB, File does not meet accessibility standards Date: 29. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03897/15

Urgent Safety Notice for Birdie Lifters, Invacare PDF, 22KB, File does not meet accessibility standards Date: 29. June 2015 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 02613/15

Corrective action for the BIRMINGHAM HIP™ RESURFACING (BHR) SYSTEM, Smith & Nephew PDF, 116KB, File does not meet accessibility standards Date: 29. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03544/15

Corrective action for the Pull Reduction Device for Percutaneous Drill Guide, Synthes GmbH PDF, 1MB, File does not meet accessibility standards Date: 29. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04012/15

Another Safety Notice for the products VIVA II, PRISMA II and MELODY II (Sleep apnea devices), Heinen + Löwenstein GmbH & Co. KG PDF, 296KB, File does not meet accessibility standards Date: 29. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03800/15

Urgent Safety Notice for the power cord of the respiration device VECTOR ET, VitalAire GmbH PDF, 154KB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 04003/15

Urgent Safety Notice for the Light Wand Stylet and Light Wand Introduction pack, Vital Signs (belonging to CareFusion) PDF, 54KB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 04004/15

Urgent Safety Notice for the Artis/Evosys Dialysis System, Gambro Dasco S.p.A PDF, 1MB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 03679/15

Corrective action for the Innova, Optima and Discovery Systems, GE Healthcare PDF, 58KB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 03677/15

Corrective action for the Dimension Vista® 500 Intelligent Lab System or Dimension Vista® 1500 Intelligent Lab System using 3.6.1 software versions, Siemens Healthcare Diagnostics PDF, 31KB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03639/15

Urgent Safety Notice for the Adaptive Servo-Ventilation (ASV) Therapy (SleepOne ProSV and SleepOne ProPSV devices), Kare Medical PDF, 373KB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03145/15

Corrective action for the Curefab CS device, Curefab Technologies GmbH PDF, 136KB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group Medical data processing (software) - others
Reference 03536/15

Synthes GmbH: Recall for the non-sterile Cortex Screw Diameter 4.5 mm, Length 105 mm, Pure Titanium PDF, 2MB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03729/15

Corrective action for the Orsiro, Sirulismus Eluting Coronary Stent System, Biotronik AG PDF, 75KB, File does not meet accessibility standards Date: 25. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03984/15

Recall for the Screwdriver blade Cross-Lock Mid 1.7, Zimmer / Normed Medizin-Technik GmbH PDF, 188KB, File does not meet accessibility standards Date: 24. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03686/15

Corrective action for the ADVIA Centaur TnI-Ultra, Siemens Healthcare Diagnostics Inc. PDF, 31KB, File does not meet accessibility standards Date: 24. June 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03494/15

Urgent Safety Notice for the NOxBOXi devices, Bedfont Scientific Ltd. PDF, 592KB, File does not meet accessibility standards Date: 24. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03687/15

Corrective action for the Abutment Retrieval Instrument and Abutment Retrieval Kit, Nobel Biocare PDF, 127KB, File does not meet accessibility standards Date: 24. June 2015 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 03969/15

Corrective action for the Tibial Alignment Guide – iAssist Knee System, Zimmer CAS PDF, 443KB, File does not meet accessibility standards Date: 24. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03982/15

Urgent Safety Notice for the Astral device, ResMed Ltd. PDF, 43KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 06324/14

Corrective action for the Camino® Intracranial Pressure Monitoring Catheter, Integra NeuroSciences PDF, 284KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03431/15

Additional Information for the CombiSets® containing Medtronic Covidien Devon™ Light Glove, Paul Hartmann AG PDF, 2MB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02871/15