Egress Capital Partners Inc. Recall: No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashews, wheat, soy, and sesame)

🇺🇸 United States

1. September 18, 2025 - Recall initiated
2. October 15, 2025 - Reported by source
3. January 16, 2026 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0017-2026

Event ID

97630

Status

Terminated

Classification

Class II

Company

Egress Capital Partners Inc.

Product description

Taproom Gourmet brand 20lb bulk "Park" Mix

Quantity

3547 cases (total)

Reason

No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashews, wheat, soy, and sesame)

Recall initiation date

September 18, 2025

Report date

October 15, 2025

Classification date

Not published in this source record

Termination date

January 16, 2026

Distribution pattern

NY, NJ, CT, CA, IL, FL

UPC, lot, and code information

SKU TG108

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 97630 with 4 other product entries in Public Health Trace.

Responsible company: Egress Capital Partners Inc.

Other recalls from Egress Capital Partners Inc.

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
New York	1
New Jersey	1
Connecticut	1
California	1
Illinois	1
Florida	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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