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GOLD STAR DISTRIBUTION INC Recall: Potential exposure of rodents and rodent activity in the distribution center.
🇺🇸 United States
OngoingClass II
Company
GOLD STAR DISTRIBUTION INC
Product
All human food products distributed from the firm. Includin…
Recall date
December 26, 2025
Source
FDA
Reason for recall
Potential exposure of rodents and rodent activity in the distribution center.
- Recall initiated
- Reported by source
Recalled products
Product description
UPC
Quantity
Lot / code information
All human food products distributed from the firm. Including but not limited to: snack foods, candy, gum, cooking oil, canned fruit and beans, honey, Dietary supplements, peanut butter, oatmeal, rice, dry peas and beans, ramen, cold cereal, hot sauce, lemon juice, crackers, canned sardines tuna and Oyster, sauces, seasonings, sugar, bottled and canned beverages, coffee and filters and creamer, tea bags, canned pasta, dates, flour, baby food
Not published in this source record
unknown
all codes of products purchased from this firm.
Distribution
IN
MN
ND
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0411-2026
Event ID
98223
Status
Ongoing
Classification
Class II
Company
GOLD STAR DISTRIBUTION INC
Product description
All human food products distributed from the firm. Including but not limited to: snack foods, candy, gum, cooking oil, canned fruit and beans, honey, Dietary supplements, peanut butter, oatmeal, rice, dry peas and beans, ramen, cold cereal, hot sauce, lemon juice, crackers, canned sardines tuna and Oyster, sauces, seasonings, sugar, bottled and canned beverages, coffee and filters and creamer, tea bags, canned pasta, dates, flour, baby food
Quantity
unknown
Reason
Potential exposure of rodents and rodent activity in the distribution center.
Recall initiation date
December 26, 2025
Report date
January 28, 2026
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
IN, MN, ND
UPC, lot, and code information
all codes of products purchased from this firm.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
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
Indiana
1
Minnesota
1
North Dakota
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.
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 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 "Ongoing." 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.
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