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Corrective action of Cell-Dyn 1700 (all serial numbers) from Abbott PDF, 101KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01940/07

Recall of the Infant Nasal CPAP Cannulas/Systems from Teleflex Medical, Hudson RCI PDF, 128KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01764/07

Information concerning a possible damage of the sterile packaging from Celon PDF, 29KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01302/07

Recall of different sterile invasive single use devices from ConMed Linvatec PDF, 534KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01607/07

Recall of the m2000 barcode readers from Abbott PDF, 76KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01832/07

Recall of patella components of the Genesis Knee System from Smith & Nephew PDF, 37KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01864/07

Recall of the 3.5 mm 90-S SERFAS Energy Suction Probe from Stryker Europe PDF, 39KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01538/07

Recall of Maverick2™ Monorail™ Balloon Catheters from Boston Scientific International S.A. PDF, 90KB, File does not meet accessibility standards Date: 05. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01725/07

Information about CENTRA Active hearing instrument from Siemens Audiologische Technik PDF, 46KB, File does not meet accessibility standards Date: 05. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01145/07

Information about HeartState F2+ defibrillator from Philips Medical Systems PDF, 85KB, File does not meet accessibility standards Date: 05. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01573/07

Recall of of MX9636 – MEDEX PDS Kids Kit from Smiths Medical International Ltd PDF, 40KB, File does not meet accessibility standards Date: 05. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01807/07

Recall of eight lot numbers of the Flexiflo 10 Fr DURA-PEG and one lot of Flexiflo 16 Fr DURA-PEG from Abbott Ireland PDF, 62KB, File does not meet accessibility standards Date: 04. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01696/07

Recall of Complete Moisture Plus from AMO Advanced Medical Optics PDF, 71KB, File does not meet accessibility standards Date: 04. June 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01830/07

Information about suprapubic bladder catheter from Tyco Healthcare Deutschland PDF, 31KB, File does not meet accessibility standards Date: 04. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00774/07

Information about Prismaflex Continuous Renal Replacement System from Gambro PDF, 91KB, File does not meet accessibility standards Date: 04. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03845/06

Information about Miroclav and System 1000 from Baxter PDF, 105KB, File does not meet accessibility standards Date: 04. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00846/07

Information about UV-Flash-Compact devices from Baxter PDF, 65KB, File does not meet accessibility standards Date: 04. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01586/07

Recall of FalcorGent Triglyceride from Menarini PDF, 45KB, File does not meet accessibility standards Date: 29. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01384/07

Information concerning the safe use of infusion sets when used in volumetric infusion pumps from CODAN PDF, 50KB, File does not meet accessibility standards Date: 25. May 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00157/05

Recall of the TriActiv® ProGuard™ Embolic Protection Systems from Kensey Nash PDF, 29KB, File does not meet accessibility standards Date: 25. May 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01198/07

Information concerning the Sprint Fidelis lead models 6930, 6931, 6948 and 6949 from Medtronic PDF, 95KB, File does not meet accessibility standards Date: 24. May 2007 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01061/07

Recall of the BD Vacutainer Safety Flow Lancets from Becton Dickinson PDF, 46KB, File does not meet accessibility standards Date: 24. May 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01160/07

Information concerning the mobile OR-table 1131.12X0, BETASTAR from Maquet PDF, 115KB, File does not meet accessibility standards Date: 24. May 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01473/07

Information concerning the Gettinge/ARJO Flusher Disinfectors, Model SP1000 “undertable unit 751” and “wall built in unit 301” from Gettinge PDF, 71KB, File does not meet accessibility standards Date: 24. May 2007 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01359/07

Recall of the S8 flow generators from ResMed PDF, 43KB, File does not meet accessibility standards Date: 24. May 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01388/07

Corrective action and recall of the Olympus Clinical Chemistry Analyser AU5400 with the software V5.3A PDF, 312KB, File does not meet accessibility standards Date: 23. May 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01582/07

Security gap in the control software of cleaning and disinfection machines type WD 280 from Belimed PDF, 55KB, File does not meet accessibility standards Date: 23. May 2007 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00351/07

Information concerning the Miele washer-disinfectors G 7823 to G 7828 PDF, 68KB, File does not meet accessibility standards Date: 23. May 2007 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01122/07

Recall of the Self Inflating Retrograde Cardioplegia Cannula from Surge Medical Solutions PDF, 26KB, File does not meet accessibility standards Date: 22. May 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01369/07