Free FDA list check · no signup, no email
Type a company name and get an answer in seconds. We check it against live openFDA enforcement and recall records (drug, device, and food) and against the FDA registered outsourcing facility (503B) list we capture on a schedule. Every match carries a name-match confidence grade, because two companies can share a name, and a match is a reason to look closer, never proof of identity or wrongdoing.
Try the company name as it appears on invoices or paperwork, for example "Central Compounding" or "Eagle Pharmaceuticals".
Checking openFDA enforcement records and the 503B snapshot…
One name, checked once
This check answers one name, one time. Suppliers pick up recalls and enforcement actions months after you onboard them. Veritura keeps every supplier and lot you rely on under continuous watch against these same FDA sources, and alerts you the day something hits. Run a document through the free check and it goes further, resolving the issuing lab against a verify-portal registry and reading the file's own metadata for edits made after the stated test date.
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What this checks, exactly. Live queries against openFDA enforcement and recall records for drugs, devices, and food (FDA updates that dataset weekly), plus a lookup against Veritura's capture of the FDA registered outsourcing facilities (503B) list; results show both FDA's own "current as of" date and our capture date. Name matches are graded by confidence (confirmed, strong, possible) and are documentation signals, not proof of identity or wrongdoing. Records where the word you typed appears only inside a product name or description, and the recalling firm's name does not match, are folded into a separate "text mentions" section; these are usually different companies whose product names contain the word, and they stay one click away so nothing is hidden. A result with no matches means none were found in these sources on these dates; it is not a clearance, and it says nothing about product quality, safety, or FDA approval. Classification (Class I, II, III) is FDA's own recall classification. This tool does not check state board actions, warning letters, or import alerts.