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United Natural Trading Inc. dba Woodstock Farms Recall: Undeclared Allergen - Milk

United States

TerminatedClass I

Company
United Natural Trading Inc. dba Woodstock Farms
Product
Fresh Direct Dark Chocolate Pretzels 7oz, Bag. 12 bags per…
Recall date
January 27, 2025
Terminated
August 8, 2025
Source
FDA

Reason for recall

Undeclared Allergen - Milk

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Fresh Direct Dark Chocolate Pretzels 7oz, Bag. 12 bags per case. Not published in this source record 99 Cases Lot#24353, best by: 06/30/25

Distribution

  • The recalled product was shipped to NY.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0552-2025
Event ID
96218
Status
Terminated
Classification
Class I
Company
United Natural Trading Inc. dba Woodstock Farms
Product description
Fresh Direct Dark Chocolate Pretzels 7oz, Bag. 12 bags per case.
Quantity
99 Cases
Reason
Undeclared Allergen - Milk
Recall initiation date
January 27, 2025
Report date
February 19, 2025
Classification date
Not published in this source record
Termination date
August 8, 2025
Distribution pattern
The recalled product was shipped to NY.
UPC, lot, and code information
Lot#24353, best by: 06/30/25
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: United Natural Trading Inc. dba Woodstock Farms

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Distribution map

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

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

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.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

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:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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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