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    Federal
Warning Letters
U.S. Department of Health & Human Services —
An index of FDA warning letters issued to companies operating in the United States. - 
  
    Federal
Clinical Investigator Inspector List (CLIIL)
U.S. Department of Health & Human Services —
The Clinical Investigator Inspection List (CLIIL) contains names, addresses, and other pertinent information gathered from inspections of clinical investigators who... - 
  
    Federal
Inactive ingredient Search for Approved Drug Products
U.S. Department of Health & Human Services —
According to 21 CFR 210.3(b)(8), an inactive ingredient is any component of a drug product other than the active ingredient. Only inactive ingredients in the final... - 
  
    Federal
Establishment Registration & Device Listing
U.S. Department of Health & Human Services —
This searchable database contains establishments (engaged in the manufacture, preparation, propagation, compounding, assembly, or processing of medical devices... - 
  
    Federal
Current and Resolved Drug Shortages and Discontinuations Reported to FDA
U.S. Department of Health & Human Services —
Information provided to FDA by manufacturers about current drugs in shortage, resolved shortages, and discontinuations of specific drug products. - 
  
    Federal
Enforcement Reports
U.S. Department of Health & Human Services —
Whereas not all recalls are announced in the media or on our Recalls press release page, all recalls montiored by FDA are included in FDA's weekly Enforcement Report... - 
  
    Federal
CDRH Inspections Database
U.S. Department of Health & Human Services —
The CDRH Inspections Database provides information about medical device inspections that were the responsibility of CDRH from 2008 to the present. - 
  
    Federal
Recalls of Food and Dietary Supplements
U.S. Department of Health & Human Services —
Food producers recall their products from the marketplace when the products are mislabeled or when the food may present a health hazard to consumers because the food... - 
  
    Federal
Public Search for Adverse Events (FOIA)
U.S. Department of Health & Human Services —
Public access allowing for public search of the FDA Adverse Events Database - 
  
    Federal
Hydrolyzed Vegetable Protein Containing Products Recalls
U.S. Department of Health & Human Services —
This list includes products subject to recall in the United States since February 2010 related to hydrolyzed vegetable protein (HVP) paste and powder distributed by... - 
  
    Federal
Fraudulent 2009 H1N1 Influenza Products Widget
U.S. Department of Health & Human Services —
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... - 
  
    Federal
Medical and Radiation Emitting Device Recalls
U.S. Department of Health & Human Services —
This database contains a list of classified medical device recalls since November 1, 2002 - 
  
    Federal
Radiation-emitting Electronic Product Codes
U.S. Department of Health & Human Services —
This database contains product names and associated information developed by the Center for all products, both medical and non-medical, which emit radiation. It... - 
  
    Federal
MedSun Reports
U.S. Department of Health & Human Services —
The Medical Product Safety Network (MedSun) is an adverse event reporting program launched in 2002. The primary goal for MedSun is to work collaboratively with the... - 
  
    Federal
Premarket Approval (PMA) Summary Review Memos for 180-Day Design Changes
U.S. Department of Health & Human Services —
A 180-day supplement is a request for a significant change in components, materials, design, specification, software, color additive, and labeling to an approved...