Food recall: Taproom Gourmet brand 20lb and 18lb bulk "Fifth Avenue" Mix
Egress Capital Partners Inc. (New Rochelle, NY) initiated this food recall on 18 Sep 2025; FDA lists 5 product records under event 97630, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 54% of the 569 food enforcement events initiated in 2025 carry the same class.
Status: Terminated, terminated 16 Jan 2026. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Egress Capital Partners Inc..
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Egress Capital Partners Inc., New Rochelle, NY.
Reason for recall
"No ingredient label. Product contains undeclared allergens (peanuts, almonds, wheat, and soy)"
Distribution
"NY, NJ, CT, CA, IL, FL"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| H-0014-2026 | Taproom Gourmet brand 20lb and 18lb bulk "Fifth Avenue" Mix | 3547 cases (total) | Class II | Terminated | 15 Oct 2025 |
| H-0015-2026 | Taproom Gourmet brand 15lb bulk "Broadway" Mix | 3547 cases (total) | Class II | Terminated | 15 Oct 2025 |
| H-0016-2026 | Taproom Gourmet brand 15lb bulk "Madison" Mix | 3547 cases (total) | Class II | Terminated | 15 Oct 2025 |
| H-0017-2026 | Taproom Gourmet brand 20lb bulk "Park" Mix | 3547 cases (total) | Class II | Terminated | 15 Oct 2025 |
| H-0018-2026 | Taproom Gourmet brand 18lb bulk "Empire" Mix | 3547 cases (total) | Class II | Terminated | 15 Oct 2025 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "No ingredient label. Product contains undeclared allergens (peanuts, almonds, wheat, and soy)"
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "NY, NJ, CT, CA, IL, FL"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 16 Jan 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.