BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Search i

Search help

  • Enter one or more search terms in the search field. Upper and lower case are not relevant.
  • As soon as you have entered three letters in the search field, various search words will be suggested from which you can choose one.
  • If you are searching for a certain group of words, put these words in double quotes. The hits will then contain the words in the order you entered, e.g. "medicines for children".
  • Multiple search terms can also be combined with the Boolean operators AND and OR. When using the operator AND, the results contain the intersection of all search terms. When using the operator OR, the hits contain one of the search terms or only individual search terms. The result set is therefore significantly larger. Please note that these operators must be written in capital letters.
  • If you receive a (too) large number of hits as a result of your search, you can narrow it down by using filters. These filter options appear to the left of the search results and are subdivided into:

    • category (e.g. safety of medicinal products, medical devices, code systems)
    • format (e.g. download, risk information, DHPCs)
    • time interval (e.g. last 30 days, older than ...)
  • Selected filters can be removed individually or all at once ("Show all results").
  • By default, search results are sorted by relevance, but they can also be sorted chronologically ("Latest entries first" or "Oldest entries first").

Enter search term

15,467 results

Filter

Results per page: 10 20 30

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

Corrective action for Central Monitors model CNS-6201, NIHON KOHDEN Corporation PDF, 649KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03606/15

Corrective action for IPS e.max Ceram and related products, Ivoclar Vivadent AG PDF, 112KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 03820/15

Corrective action for the products VIVA II, PRISMA II and MELODY II (Sleep apnea devices), anamed GmbH & Co. KG PDF, 195KB, 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 03361/15

Recall for the Celsite® Access Ports, B. Braun Medical France PDF, 649KB, File does not meet accessibility standards Date: 23. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03811/15

Important Safety Notice for Dräger monitor holders with AC2000, Dräger Medical GmbH PDF, 1MB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03627/15

Corrective action for the product AMICA Probe, HS Hospital Service SpA PDF, 2MB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02903/15

Corrective action for Telemetry Systems, NIHON KOHDEN Corporation PDF, 636KB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03631/15

Urgent Safety Notice for the EIT PLIF Shaver, EIT Emerging Implant Technologies GmbH PDF, 830KB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03757/15

Corrective Action for OxiMax™ N-65 Handheld Pulse Oximeters and OxiMax™ N-560 Pulse Oximeters, Covidien Deutschland GmbH PDF, 250KB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03040/15

Corrective action for the Digital Radiography X-Ray System DX-D 100 Type 5410 or DX-D 100 Wireless Type 5411, Agfa HealthCare NV PDF, 85KB, File does not meet accessibility standards Date: 22. June 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 03593/15

Recall of Alcon ACCURUS® STANDALONE VITREOUS PROBES, Alcon Pharma GmbH PDF, 159KB, File does not meet accessibility standards Date: 18. June 2015 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 03643/15

Corrective action for the RAPIDLab 1260 and RAPIDLab 1265 Blood Gas analyzers, Siemens Healthcare Diagnostics PDF, 218KB, File does not meet accessibility standards Date: 18. June 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03147/15

Corrective action for the Shiley™ Neonatal and Pediatric products, Covidien LLC PDF, 2MB, File does not meet accessibility standards Date: 18. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03134/15

Recall for Guide Wire 2.8mm, Length 180mm with Thread, Synthes GmbH PDF, 2MB, File does not meet accessibility standards Date: 18. June 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03835/15

Corrective action for optimys stems standard and lateral, Mathys Ltd. Bettlach PDF, 40KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02698/15

Recall for various orthopedic products, Biomet Orthopedics PDF, 261KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03197/15

Corrective action - Manufacturer IFU replacement for the VariLase® Endovenous Laser Fibers and Procedure Kits, Vascular Solutions Inc. PDF, 139KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - laser technology
Reference 02574/15

Recall for the product ProcedurePak®, Mölnlycke Health Care PDF, 75KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 03759/15

Boston Scientific: Corrective action for specific CLEARSIGN II Amplifiers, which are part of the LABSYSTEM PRO EP Recording System PDF, 229KB, File does not meet accessibility standards Date: 17. June 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03678/15