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

15,455 results

Filter

Results per page: 10 20 30

Lot Recall of a TEP inlay, Stryker PDF, 30KB, File does not meet accessibility standards Date: 28. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05992/11

Urgent Recall of the CSLP System Ø 3.0mm Drill Bits and the Fixation Sleeve, Synthes GmbH PDF, 243KB, File does not meet accessibility standards Date: 28. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05407/12

Urgent Recall of the Vectra System graduated 2.5mm Drill Bit and the Adjustable Drill Stop, Synthes GmbH PDF, 255KB, File does not meet accessibility standards Date: 28. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05406/12

Lot Recall of the Paediatric Arterial Cannula, MAQUET Cardiopulmonary PDF, 361KB, File does not meet accessibility standards Date: 27. August 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03316/12

Recall for HOSPIRA Li-ion GEMSTAR™-Dockingstation PDF, 779KB, File does not meet accessibility standards Date: 27. August 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 03765/11

Safety Notice for DePuy's cemented polished CoCr alloy femoral hip stems combined with MoM articulation, DePuy PDF, 2MB, File does not meet accessibility standards Date: 27. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02877/12

Safety Notice for Carescape Monitor B850, GE Healthcare Finland Oy PDF, 67KB, File does not meet accessibility standards Date: 24. August 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 04849/12

Urgent Safety Notice for the Delta Motion Acetabular Implant, DePuy PDF, 3MB, File does not meet accessibility standards Date: 24. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03364/12

Safety Notice concerning malfunction of the Semikron Diode of all SL75/5 Linacs, Elekta PDF, 120KB, File does not meet accessibility standards Date: 24. August 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 05377/12

Recall for the E1-Tapered 10° Liner 32/39, Biomet PDF, 1MB, File does not meet accessibility standards Date: 24. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05201/12

Recall for infusion pump administration sets for use with Curlin ambulatory infusion pumps, Moog PDF, 457KB, File does not meet accessibility standards Date: 24. August 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 02588/12

Recall of several Sharpoint Slit Knives, Surgical Specialties Puerto Rico dba Angiotech PDF, 614KB, File does not meet accessibility standards Date: 24. August 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 05453/12

Recall of plug power supplies used for chargers for rechargeable hearing aids, Siemens Audiologische Technik GmbH PDF, 118KB, File does not meet accessibility standards Date: 24. August 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - ENT equipment
Reference 03124/12

Recall Information concerning the Qufora Irrigation System, MBH-International A/S PDF, 28KB, File does not meet accessibility standards Date: 23. August 2012 Topics: Medical devices Type: Customer information

Product group Physical therapy - hydrotherapy
Reference 02832/12

Recall of two lots of the Taperloc Femoral Stem, Biomet UK Ltd. PDF, 830KB, File does not meet accessibility standards Date: 23. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05604/11

Safety Notice for Infusionpumps: Volumed µVP7000 Premium / Classic Plus / Lite and Syramed µSP6000 Premium / Classic Plus, Arcomed AG PDF, 3MB, File does not meet accessibility standards Date: 23. August 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 03864/12

Safety Notice for XPREZZON-Bedside-Monitor, Spacelabs Healthcare PDF, 94KB, File does not meet accessibility standards Date: 23. August 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 04449/12

Recall of DGP-HP High-Power single use grounding pads and Cool-tip™ RFA Electrode Kits, Covidien PDF, 222KB, File does not meet accessibility standards Date: 22. August 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05367/12

Lot Recall of the blood collection stopcock ArterioGuard, Codan pvb Critical Care GmbH PDF, 749KB, File does not meet accessibility standards Date: 22. August 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion kits
Reference 05325/12

Lot Recall for the S.M.A.R.T. ® Nitinol Stent System and S.M.A.R.T. ® CONTROL ® Nitinol Stent System, Cordis PDF, 235KB, File does not meet accessibility standards Date: 22. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 02503/12

Lot Recall of a syringe, Pluradent AG & Co. KG PDF, 974KB, File does not meet accessibility standards Date: 21. August 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 05229/12

Corrective Action for ADVIA Centaur and ADVIA Centaur XP Multi Diluent 1, Siemens PDF, 164KB, File does not meet accessibility standards Date: 21. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05195/12

Recall for ImmunoComb II HAV IgM, Orgenics PDF, 94KB, File does not meet accessibility standards Date: 21. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04813/12

Corrective Action for the HALOFLEX Energy Generator, BARRX Medical, Inc. PDF, 60KB, File does not meet accessibility standards Date: 20. August 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05299/12

Safety Notice concerning the KleenSpec® Disposable Vaginal Specula, Welch Allyn Inc. PDF, 604KB, File does not meet accessibility standards Date: 20. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - gynaecology
Reference 05373/12

Urgent Safety Notice for the use of the Agility™ and Apex™-Systems, Elekta PDF, 311KB, File does not meet accessibility standards Date: 20. August 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 05160/12

Recall for LIFECODES PAK 12, PAKAUTO, PAKPLUS & PAK2-LE, Gen-Probe PDF, 2MB, File does not meet accessibility standards Date: 20. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05231/12

Recall of the power supply DT50 manufactured by Friwo and which is used with the Pari Sole N inhalation device, Pari GmbH PDF, 268KB, File does not meet accessibility standards Date: 17. August 2012 Topics: Medical devices Type: Customer information

Product group Physical therapy - inhalation therapy
Reference 03411/11

Recall of the Symplicity® Catheter (Model RDN006), Medtronic PDF, 73KB, File does not meet accessibility standards Date: 17. August 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05121/12

Recall for the Torque Wrench XIA3-Mantis Redux-Specialty Audible, Stryker Spine Bordeaux PDF, 37KB, File does not meet accessibility standards Date: 17. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05349/12