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U.S. Department of Health and Human Services

About FDA

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 - 2011

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TimeTargetNumber
Oct 2010N/A29
Nov 2010N/A31
Dec 2010N/A29
Jan 2011N/A22
Feb 2011N/A23
Mar 2011N/A29
Apr 2011N/A32
May 2011N/A31
Jun 2011N/A19
Jul 2011N/A30
Aug 2011N/A37
Sep 2011N/A32

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

Fiscal Year - 2011

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TimeTargetNumber
Oct 2010N/A101
Nov 2010N/A108
Dec 2010N/A112
Jan 2011N/A114
Feb 2011N/A118
Mar 2011N/A121
Apr 2011N/A128
May 2011N/A130
Jun 2011N/A132
Jul 2011N/A140
Aug 2011N/A145
Sep 2011N/A150

FY 2011 Overall: 150

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.