US product recalls — openFDA
A free reference of FDA enforcement (recall) actions across drug, food and device, from the FDA's open data. The high-severity markers surfaced are a Class I recall (the FDA's most serious class — a reasonable probability that use will cause serious adverse health consequences or death) and a still-ongoing recall. Lower-class, resolved recalls are not surfaced. A recall is a contestable, often firm-initiated safety action — "subject to a Class I recall on record", never "dangerous" or "unsafe".
Source: openFDA enforcement (drug / food / device), refreshed weekly · open.fda.gov.
On record
| On record | count |
|---|---|
| Recalling firms | 9,617 |
| Class I recalls (most serious) | 2,407 |
| Ongoing recalls surfaced | 14,676 |
| High-severity events surfaced | 32,898 |
| Recall history on record | 2006–2026 |
The value is cross-register
This lens compounds when joined to the other registers on the same proven entity. Browse the cross-register overlaps, resolve a company in the dossier, or read how entities are resolved across registers.
Aggregated and non-nominative: individual records and companies are not named on this page. Descriptive counts only — no conclusions.