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U.S. Department of Health and Human Services

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Number of recall recommendations during the month entered in the Recall Enterprise System (RES) resulting from environmental positives

Dictionary: This measure captures the number of product recalls due to environmental contamination in the manufacturing, storage, or transit facilities that result when current good manufacturing practices (cGMPS) are not followed. cGMPs ensure that FDA regulated products are manufactured under safe and sanitary conditions. Environmental controls are part of an overall approach to cGMPS.

Information is current as of March 31, 2014.

Fiscal Year - 2013

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TimeTargetNumber
Oct 2012N/A39
Nov 2012N/A1
Dec 2012N/A0
Jan 2013N/A0
Feb 2013N/A0
Mar 2013N/A0
Apr 2013N/A1
May 2013N/A1
Jun 2013N/A9
Jul 2013N/A0
Aug 2013N/A0
Sep 2013N/A0

FY 2013 Total: 51

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.