FDA can recall a cosmetic and suspend the facility
FDA can order a mandatory recall of an adulterated or misbranded cosmetic likely to cause serious harm, and can suspend a facility’s registration, after which distributing product from that facility in the United States is a prohibited act.
One suspended registration stops the whole line, not one SKU, so your manufacturer’s compliance is your commercial risk.
95 of a possible 97Tier A, primary document or measured outcome. Nothing at this tier is allowed past 97, however good it looks.
Verified August 4, 2026Rechecked every 180 days, next by January 31, 2027.
Held since August 4, 2026A rule, law or policy that limits what you may do or say. The earliest date we are willing to say this held. It may well have been true before that; we do not backdate a record past the evidence we have read. Supported, version 1.
This entry is wrong if
FDA states it lacks mandatory recall authority for cosmetics, or that distribution may continue after a registration suspension.
Written before the record was published, not after. If you can show this, send it to hello@tryorbt.com and the correction goes on the record with the entry.
Evidence
- Tier Aregulation
U.S. Food and Drug Administration: Modernization of Cosmetics Regulation Act of 2022 (MoCRA)
Mandatory Recall Authority: If the agency determines that there is a reasonable probability that a cosmetic is adulterated or misbranded and the use of or exposure to the cosmetic will cause serious adverse health consequences or death, FDA has the authority to order a mandatory recall if the responsible person refuses to do so voluntarily. [...] If a facility’s registration is suspended, it is a prohibited act to distribute or sell (or otherwise introduce or deliver into commerce) in the United States cosmetic products from the facility.
Two passages from the same page, one on recall and one on suspension. The bracket marks where the page runs on between them.
Read 2026-08-04 · Public domain · page hash
8cc8da80f378
History
- v1created
Initial entry from primary regulator text, read 2026-08-04.
Append-only. Nothing in this list is edited or removed once written, including the entries that record our own mistakes. Every change to every record is on the corrections page, and the same log is in entries.json under revisions.
Cite this entry
“FDA can recall a cosmetic and suspend the facility”, The Orbt Market Index 0.1.0, entry omr:us:mocra-recall-and-suspension-authority, retrieved September 9, 2026, https://tryorbt.com/markets/entry/us--mocra-recall-and-suspension-authority. Dataset: https://doi.org/10.5281/zenodo.22679129
Orbt, "FDA can recall a cosmetic and suspend the facility," Orbt Market Index, entry omr:us:mocra-recall-and-suspension-authority, verified August 4, 2026, https://tryorbt.com/markets/entry/us--mocra-recall-and-suspension-authority.
@misc{orbt-us-mocra-recall-and-suspension-authority,
title = {FDA can recall a cosmetic and suspend the facility},
author = {{Orbt}},
year = {2026},
doi = {10.5281/zenodo.22679129},
note = {The Orbt Market Index 0.1.0 (dataset DOI 10.5281/zenodo.22679129), entry omr:us:mocra-recall-and-suspension-authority. Verified 2026-08-04},
howpublished = {\url{https://tryorbt.com/markets/entry/us--mocra-recall-and-suspension-authority}},
license = {Orbt Index Public Licence. Free to quote and cite; not to redistribute}
}For a deck, a brief or a chat.
Free to quote, cite and act on. Not to resell or redistribute — the sources ask that of us, and each one’s terms are named. Machine-readable: entries.json carries this record under the id omr:us:mocra-recall-and-suspension-authority, with the same evidence and falsifier.
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