DistributorLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 4 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Walmart and its 1 subsidiaries with 5 510(k) clearances, 4 drug recalls and 4 warning letters. The most recent is a warning letter dated Oct 1, 2026: Warning letter: Unapproved new drug.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Walmart and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Oct 1, 2026 | Warning letter: Unapproved new drugCDER | Warning letters |
| Jul 25, 2024 | Warning letter: MDR reporting, Unapproved new drugCDER | Warning letters |
| Aug 18, 2023 | Warning letter: Unapproved new drugCDER | Warning letters |
| Oct 28, 2022 | Warning letter: Unapproved new drug, LabelingCDER | Warning letters |
| Feb 9, 2022 | Avaphinal Maximum Male Enhancement Sexual Pills, 2000 MG*, packaged in 10 Capsules per carton.Class I · Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil, an ingredient found in FDA ap | Drug recalls |
| Oct 25, 1995 | SUNGLASSESK954639 · HQY | 510(k) clearances |
| Jan 5, 1995 | SUNGLASSESK945817 · HQY | 510(k) clearances |
| Jan 5, 1995 | SUNGLASSESK945819 · HQY | 510(k) clearances |
| Jan 5, 1995 | SUNGLASSESK945818 · HQY | 510(k) clearances |
| May 9, 1994 | SUNGLASSESK941680 · HQY | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
