Food, drugs, devices › New Age International, Inc.
Food recall: Signature brand Enoki Mushroom; 200g; clear plastic package
FDA enforcement event 97732 is a food recall by New Age International, Inc. of Brooklyn, NY, initiated 29 Sep 2025 and classified Class I, with 1 product record.
FDA defines Class I as a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. 37% of the 569 food enforcement events initiated in 2025 carry the same class.
Status: Terminated, terminated 11 Feb 2026. Initiation: voluntary: firm initiated. New Age International, Inc. has 3 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
New Age International, Inc., Brooklyn, NY.
Reason for recall
"Product may be contaminated with Listeria monocytogenes."
Distribution
"NY"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| H-0026-2026 | Signature brand Enoki Mushroom; 200g; clear plastic package | 175 boxes | Class I | Terminated | 15 Oct 2025 |
Context
Other enforcement events for New Age International, Inc.
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 11 Mar 2025 | Daily Veggies Enoki Mushroom; Product of Korea; Net WT. 200 g (7.05 oz); KEEP REFRIGERATED; Cook through before | Food | Class I | 1 |
| 11 Dec 2024 | Daily Veggies Enoki Mushroom, 200g Product of Korea UPC Codes: 8809159458890 | Food | Class I | 1 |
All 3 events for New Age International, Inc.
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Product may be contaminated with Listeria monocytogenes."
What does Class I mean?
FDA classifies recalls by relative degree of health hazard. Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
Where was the product distributed?
FDA's distribution pattern field reads: "NY"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 11 Feb 2026. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.