Conah Organic Enoki Mushrooms; 200 g (7.05 oz.) clear package with orange bottom UPC 8 51511 00770 1 Distributed by: Marquis Worldwid...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0749-2021.
California Department of Public Health sampled Conah Organic Enoki mushrooms with a positive result for Listeria monocytogenes.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0749-2021.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Marquis Worldwide Specialty Inc or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0749-2021.
Marquis Worldwide Specialty Inc
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Marquis Worldwide Specialty Inc Recall FAQ
Marquis Worldwide Specialty Inc is the subject of a food safety report: Conah Organic Enoki Mushrooms; 200 g (7.05 oz.) clear package with orange bottom UPC 8 51511 00770 1 Distributed by: Marquis Worldwid.... The notice was published on May 28, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 1,320 units are potentially affected.