Main There are many offices involved in the process of posting a firm’s Class 1 recall press release on FDA.gov. A final press release is received by the District and sent to OE for approval and posting. Once OE receives the final press release from the District, it is reviewed by OE and sent to ORA web team for formatting. The formatted version is sent back to OE for approval. Once approved, the ORA web team is notified by OE and posts the press release to FDA.gov. OE will measure the time from OE’s receipt of the final draft from the District until OE notifies the ORA web team of the approval for posting with the goal of 100% completed within 24 hours. The actual posting of the release to the website is not in OE’s control and may be affected by IT issues and therefore will not be included in this timeframe. OE’s goal is to ensure it meets its responsibilities in a timely manner. OE will document the reason(s) for any press releases received and not approved for posting within 24 hours and will take corrective action as needed. <i>Information is current as of February 12, 2013.</i> Percent column 0 100 Measure was implemented starting January 2011.

Jan 2011 100 97 Feb 2011 100 85 Mar 2011 100 93 Apr 2011 100 87 May 2011 100 93 Jun 2011 100 93 Jul 2011 100 100 Aug 2011 100 100 Sep 2011 100 100 100

Oct 2011 100 100 Nov 2011 100 100 Dec 2011 100 100 Jan 2012 100 100 Feb 2012 100 100 Mar 2012 100 100 Apr 2012 100 100 May 2012 100 100 Jun 2012 100 100 Jul 2012 100 100 Aug 2012 100 100 Sep 2012 100 100

Oct 2012 100 Nov 2012 100 Dec 2012 100 Jan 2013 Feb 2013 Mar 2013 Apr 2013 May 2013 Jun 2013 Jul 2013 Aug 2013 Sep 2013 http://www.fda.gov/AboutFDA/Transparency/track/ucm204013.htm FDA-TRACK ORA Dashboard ਍††਍਍਍਍਍਍਍