CENTRO DI DOCUMENTAZIONE SUI DISPOSITIVI MEDICI

FDA posts consumer information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious health problems or death. Use the yearly lists to find information about Class I medical device recalls and some Class II and III recalls of interest to consumers. The links give details about what to do if you own or use one of these products. Please note that FDA now lists medical device recall notices by the date that it posts the recall rather than the recall initiation date.  You can find the date that a firm initiated a recall in the text of the recall notice. Link>   Recent Medical Device Recalss Updated  10/17/14

Short name: Medical devices Base: Council Directive 93/42/EEC of 14 June 1993 concerning medical devices OJ L 169 of 12 July 1993 Modification: Directive 93/68/EEC  [CE Marking] Directive 98/79/EC  of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices Directive 2000/70/EC  of the European Parliament and of the Council of 16 November 2000 amending Council Directive 93/42/EEC as regards medical devices incorporating stable derivates of human blood or human plasma Directive 2001/104/EC  of the European Parliament and of the Council of 7 December 2001 amending Council Directive 93/42/EEC concerning medical devices Directive 2007/47/EC  of the European Parliament and of the Council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices a...