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U.S. Department of Health and Human Services

About FDA

Cumulative number of technical analyses of postmarket device problems and performance completed

Cumulative FY 2011 Target: 130 by 9/30/2011

Dictionary: Postmarket device problems and performance issues constitute one of CDRH’s primary public health priorities. Typically, the appearance of such problems begins with many ambiguities and gaps in understanding exactly what happened in the reported incident(s) and, more importantly, why. The technical analyses are used to assess the hazards, determine the adequacy of proposed corrective actions, determine appropriate test methods, and develop case strategies for reported problems.

Information is current as of August 31, 2013

Fiscal Year - 2011

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Cumulative FY 2011 Target: 130 by 9/30/2011

TimeCumulative Annual TargetCumulative Number
Oct 20101308
Nov 201013017
Dec 201013026
Jan 201113051
Feb 201113058
Mar 201113072
Apr 201113080
May 201113094
Jun 2011130108
Jul 2011130125
Aug 2011130142
Sep 2011130160

FY 2011 Total: 160

Number of technical analyses of postmarket device problems and performance completed during the month

Cumulative FY 2011 Target: 130 by 9/30/2011

Fiscal Year - 2011
Skip graphic and jump to text data.

Cumulative FY 2011 Target: 130 by 9/30/2011

TimeTargetNumber
Oct 2010N/A8
Nov 2010N/A9
Dec 2010N/A9
Jan 2011N/A25
Feb 2011N/A7
Mar 2011N/A14
Apr 2011N/A8
May 2011N/A14
Jun 2011N/A14
Jul 2011N/A17
Aug 2011N/A17
Sep 2011N/A18

FY 2011 Total: 160

Glossary

Note: The data provided on this website is produced on an ongoing basis for performance management purposes and is subject to change due to updates of preliminary estimates, corrections, or other reasons. In addition, FDA may change the type or amount of data provided on this website at any time. Information marked as "Completed" may include measures and/or key projects for which activities are ongoing but no longer tracked as part of FDA-TRACK.