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

14,984 results

Results per page: 10 20 30

Corrective action for the CARDIOSAVE® Hybrid Intra-Aortic Balloon Pump (IABP), Maquet / Datascope Corp. PDF, 53KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07638/14

Recall for LENTIS HydroSmart foldable Intraocular lenses in glass vials, Oculentis GmbH PDF, 39KB, File does not meet accessibility standards Date: 08. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 08056/14

Recall for the ARROW® Continuous Nerve Block Needle, ARROW International Inc. PDF, 218KB, File does not meet accessibility standards Date: 08. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - injection kits
Reference 07693/14

Recall for the Guide Wire Semislip, Urotech PDF, 31KB, File does not meet accessibility standards Date: 08. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07811/14

Urgent Safety Notice for the DRX-Revolution Mobile X-Ray System, Carestream Health, Inc. PDF, 132KB, File does not meet accessibility standards Date: 08. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - mobile radiological diagnostic facilities
Reference 07851/14

DePuy Synthes: Recall for the Cannulated Screw Ø 3.5 mm, self-drilling, length 40/13 mm, Titan PDF, 900KB, File does not meet accessibility standards Date: 05. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07908/14

Recall for KimVent* Microcuff* Subglottic Suctioning Endotracheal Tubes, Halyard Health, Inc. (formerly Kimberly-Clark Health Care) PDF, 261KB, File does not meet accessibility standards Date: 05. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07931/14

Recall for the Shaver Blades, straight/curved, single use and sterile, SPIGGLE & THEIS Medizintechnik GmbH PDF, 4MB, File does not meet accessibility standards Date: 05. December 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 07841/14

Recall for the product "Setzkopf Primaro-Pfanne", OHST Medizintechnik AG PDF, 7MB, File does not meet accessibility standards Date: 05. December 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07166/14

Corrective Action for Rhythmia Medical’s IntellaMap Orion™ High Resolution Mapping Catheter, Boston Scientific International S.A. PDF, 181KB, File does not meet accessibility standards Date: 05. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07901/14

Urgent Safety Notice for the ATTUNE® INTUITION™ Impaction Handle, ATTUNE® INTUITION™ Impactors, DePuy Synthes PDF, 584KB, File does not meet accessibility standards Date: 05. December 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07929/14

Corrective action for the Oxoid Legionella BCYE Growth Supplement, Thermo Fisher Scientific Microbiology Basingstoke PDF, 38KB, File does not meet accessibility standards Date: 04. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06839/14

Recall for the Protégé Rx Tapered Carotid Stent System, Covidien PDF, 90KB, File does not meet accessibility standards Date: 04. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 08063/14

Recall for HeartWare® Batteries of the HeartWare® Ventricular Assist System, HeartWare, Inc. PDF, 217KB, File does not meet accessibility standards Date: 04. December 2014 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 02492/14

Corrective action for the BrightView SPECT, BrightView X and BrightView XCT Systems, Philips Healthcare PDF, 358KB, File does not meet accessibility standards Date: 04. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 07766/14

Urgent Safety Notice for the ATTUNE® Intuition Distal Femoral Jig, DePuy Synthes PDF, 700KB, File does not meet accessibility standards Date: 04. December 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07579/14

Recall of the Fluoron Gas Tamponade EasyGas SF6, Fluoron GmbH PDF, 3MB, File does not meet accessibility standards Date: 04. December 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - other medical devices for ophthalmological purposes
Reference 07966/14

Urgent Safety Notice for the Healon EndoCoat Opthalmic Viscosurgical Device, AMO Ireland PDF, 34KB, File does not meet accessibility standards Date: 03. December 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - liquid media for ophthalmological purposes
Reference 07603/14

Safety Notice for the Biograph mCT- and Biograph mCT Flow systems, running VG50A equipped with the Adaptive 3D Intervention option, Siemens Medical Solution USA, Inc. PDF, 767KB, File does not meet accessibility standards Date: 03. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 07789/14

Safety Notice for Atlantis Profile Abutments (Ti), DENTSPLY Implants PDF, 76KB, File does not meet accessibility standards Date: 03. December 2014 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 01895/13