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CriticalFDAfda-F-0826-2022LISTERIA

Fresh Enoki Mushrooms 5.25oz/150 g/ 34 packages per case UPC: 001958939091 Distributed by Concord Farms, Vernon, CA Do not eat ...

⚠ 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.

Category
Units Affected
800
Recall Date
February 9, 2022
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0826-2022.

California Department of Public Health sampled product and found it to contain Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0826-2022.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Concord Farms, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-0826-2022.

Concord Farms, Inc.

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 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.

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Concord Farms, Inc. Recall FAQ

Concord Farms, Inc. is the subject of a food safety report: Fresh Enoki Mushrooms 5.25oz/150 g/ 34 packages per case UPC: 001958939091 Distributed by Concord Farms, Vernon, CA Do not eat .... The notice was published on February 9, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 800 units are potentially affected.