Taproom Gourmet brand 20lb and 18lb bulk "Fifth Avenue" Mix
Summary
The FDA issued a Class II for Taproom Gourmet brand 20lb and 18lb bulk "Fifth Avenue" Mix by Egress Capital Partners Inc.. Reason: No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashew, and soy).
Details
Source
Food Recall
External ID
H-0014-2026
Action Date
2025-10-15
Status
Terminated
Category
food
Product Description
Taproom Gourmet brand 20lb and 18lb bulk "Fifth Avenue" Mix
Lot/Code Info: SKU TG107
Quantity Affected: 3547 cases (total)
Reason for Recall
No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashew, and soy)
Distribution
NY, NJ, CT, CA, IL, FL
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-18
Company
New Rochelle, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Egress Capital Partners Inc. has 5 FDA actions in our database, including 5 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Egress Capital Partners Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Egress Capital Partners Inc. have FDA actions?
Egress Capital Partners Inc. has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0014-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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