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FDA Pistachio Product Recalls Widget |
Contains data for FDA pistachio product recalls since March 2009. |
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Health and Nutrition |
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FDA Peanut Product Recalls |
Contains data for FDA peanut product recalls since January 2009. |
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Health and Nutrition |
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FDA Peanut Product Recalls Widget |
Contains data for FDA peanut product recalls since January 2009. |
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FDA Plainview Milk Cooperative Ingredient Recall |
Contains data for the FDA Plainview Milk Cooperative Ingredient Recall since June 2009. |
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Fraudulent 2009 H1N1 Influenza Products |
This list is intended to alert consumers about Web sites that are or were illegally marketing unapproved, uncleared, or unauthorized products in relation to the 2009 H1N1 Flu Virus (sometimes referred to as the "swine flu" virus). |
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FDA |
Health and Nutrition |
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Fraudulent 2009 H1N1 Influenza Products Widget |
This list is intended to alert consumers about Web sites that are or were illegally marketing unapproved, uncleared, or unauthorized products in relation to the 2009 H1N1 Flu Virus (sometimes referred to as the "swine flu" virus). |
HHS |
FDA |
Health and Nutrition |
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FDA Abbott Infant Formula Recall |
On September 22, 2010, Abbott issued a voluntary recall of certain Similac powdered infant formula after identifying a common warehouse beetle (both larvae and adults) in the finished product at their Sturgis, Michigan plant. The company immediately put all product manufactured at the Michigan plant on hold and ceased manufacturing at that location. FDA has advised against consumption of the recalled product and urged consumers to follow the manufacturer's instructions for reporting and returning the formula. |
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FDA Drug Label Data |
This file contains the data elements used for searching the FDA Online Data Repository including proprietary name, active ingredients, marketing application number or regulatory citation, National Drug Code, and company name.<br /> |
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FDA Online Label Repository |
The drug labels and other drug-specific information on this Web site represent the most recent drug label information companies have submitted to the Food and Drug Administration (FDA).<br /> |
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Adverse Event Reporting System (AERS) |
The Adverse Event Reporting System (AERS) is a computerized information database designed to support the FDA's post-marketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses AERS to monitor for new adverse events and medication errors that might occur with these marketed products.<br /> Reporting of adverse events from the point of care is voluntary in the United States. FDA receives some adverse event and medication error reports directly from health care professionals (such as physicians, pharmacists, nurses and others) and consumers (such as patients, family members, lawyers and others). Healthcare professionals and consumers may also report these events to the products' manufacturers. If a manufacturer receives an adverse event report, it is required to send the report to FDA as specified by regulations. <br /> The files listed on this page contain raw data extracted from the AERS database for the indicated time ranges and are not cumulative.<br /> Users of these files need to be familiar with creation of relational databases using applications such as ORACLE, Microsoft Office Access, MySQL and IBM DB2 or the use of ASCII files with SAS analytic tools.<br /> A simple search of AERS data cannot be performed with these files by persons who are not familiar with creation of relational databases. |
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