Recall Ledger

"***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch recall (Pack'n Fresh LLC)

FoodClass IIOngoing

Summary: Pack'n Fresh LLC is recalling "***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch, pouches packed in brown paperboard cartons (600 packets/carton), Carton label reads in part as "***Hondashi 0.25oz*600bags/ctn, Ingredients: salt, sodium glutamate, bonito, cornstarch, maltodextrin, water, flavored sodium nuc. Reason: Allergen missing from contains statement: fish.

What is being recalled

"***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch, pouches packed in brown paperboard cartons (600 packets/carton), Carton label reads in part as "***Hondashi 0.25oz*600bags/ctn, Ingredients: salt, sodium glutamate, bonito, cornstarch, maltodextrin, water, flavored sodium nucleotide, glucose, soybean protein powder Allergen: Soybean, 1025 Ave S, Ste 150, Grand Prairie, TX 75050***"

Why

Allergen missing from contains statement: fish

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

NJ, CA (states named: California, New Jersey)

How to tell if yours is affected

Lot #: OA00822015 Best By: 9/21/2024 Lot #: Z2412426123 Best By: 5/3/2026 Lot #: Z2424526232 Best By: 9/21/2026 Lot #: Z2435226351 Best By: 12/17/2026 Lot #: Z2507827077 Best By: 7/8/2027 Lot #: Z2524927248 Best By: 9/5/2027

What to do

Check the product name and the codes above against what you have. If they match, do not eat or use it. Throw it away or return it to the store where you bought it, and contact the recalling company with questions.

Recall facts

Recall numberH-1194-2026
CategoryFood
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedJuly 9, 2026
ReportedAugust 12, 2026
CompanyPack'n Fresh LLC
Company locationGrand Prairie, TX, United States
Initiated byVoluntary: Firm initiated
Quantity109,600 units

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Official FDA record