Enoki Mushroom, 150g clear plastic bag with orange bottom; UPC 085412004020 Product of Korea Do no consume Raw Distributed by Rainfield...
⚠ 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-0748-2021.
California Department of Public Health sampled Enoki mushrooms at retail 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-0748-2021.
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 Rainfield Marketing Group 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-0748-2021.
RAINFIELD MARKETING GROUP
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.
Rainfield Marketing Group Recall FAQ
Rainfield Marketing Group is the subject of a food safety report: Enoki Mushroom, 150g clear plastic bag with orange bottom; UPC 085412004020 Product of Korea Do no consume Raw Distributed by Rainfield.... The notice was published on May 28, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 1,200 units are potentially affected.