About this reference

Every food and dietary supplement recall published by the U.S. Food & Drug Administration is made public through the openFDA project. This site is a fast, searchable mirror — every recall, every class, every firm.

What's a Class I recall?

FDA classifies recalls by severity of the health risk:

• Class I — reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
• Class II — consumption may cause temporary or medically reversible adverse health consequences; probability of serious consequences is remote.
• Class III — consumption is not likely to cause adverse health consequences.

Data source

All records sourced from openFDA's food enforcement endpoint via its published JSON bulk export. Refreshed weekly.

Not legal or medical advice

If you believe you were made ill by a recalled product, contact your healthcare provider and consider reporting the illness to the FDA. If you have a recalled product, follow the recall notice or contact the manufacturer directly.