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U.S. Department of Health and Human Services

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Number of unique firm names entered into CAERS from mandatory reports, by month

Dictionary: FDA’s Center for Food Safety and Applied Nutrition Adverse Event Reporting System (CAERS) captures data on adverse events and product complaints reported about food, dietary supplements or cosmetics. These reports come from consumers, health professionals, the industry or others. Information from reports on adverse events experienced by individuals aids FDA in detecting problems with the safety of these products.

Fiscal Year - 2010

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TimeTargetNumber
Oct 2009N/A34
Nov 2009N/A28
Dec 2009N/A22
Jan 2010N/A25
Feb 2010N/A22
Mar 2010N/A33
Apr 2010N/A24
May 2010N/A28
Jun 2010N/A32
Jul 2010N/A27
Aug 2010N/A25
Sep 2010N/A15

Cumulative number of unique firm names entered into CAERS from mandatory reports, across months

Fiscal Year - 2010

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TimeTargetNumber
Oct 2009N/A34
Nov 2009N/A49
Dec 2009N/A55
Jan 2010N/A62
Feb 2010N/A65
Mar 2010N/A74
Apr 2010N/A78
May 2010N/A82
Jun 2010N/A85
Jul 2010N/A87
Aug 2010N/A92
Sep 2010N/A93

FY 2010 Overall: 93

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.