Class ITerminatedVoluntary: Firm initiated
New Age International, Inc.: food recall H-0026-2026
New Age International, Inc. of Brooklyn, NY recalled Signature brand Enoki Mushroom; 200g; clear plastic package. Reason: Product may be contaminated with Listeria monocytogenes. The FDA listed it as Class I in its Enforcement Report dated Oct 15, 2025; distribution: New York.
Record status as published: Terminated (terminated Feb 11, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Signature brand Enoki Mushroom; 200g; clear plastic package
- Product quantity
- 175 boxes
- Reason for recall
- Product may be contaminated with Listeria monocytogenes.
- Codes, lots and dates on the package
- GGN: 4063061794758
- Distribution pattern
- NY
- Recalling firm
- New Age International, Inc., Brooklyn, NY
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Sep 29, 2025 |
| Classified by the FDA | Oct 7, 2025 |
| Published in the Enforcement Report | Oct 15, 2025 |
| Terminated | Feb 11, 2026 |
Other recalls by New Age International, Inc.
- F-0646-2025 · Mar 26, 2025 · Class I — Contaminated with Listeria monocytogenes
- F-0398-2025 · Jan 22, 2025 · Class I — may be contaminated with Listeria monocytogenes
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OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0026-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.