FDA recall, , Moderate risk
Pack'n Fresh Hondashi Seasoning
Hondashi 0.25oz seasoning lacks a fish allergen statement.
Summary by Recall Canary from the FDA notice
What happened
Pack'n Fresh LLC of Grand Prairie, Texas, recalled Hondashi 0.25oz seasoning packed in silver plastic/metallic pouches, with pouches in brown paperboard cartons, because the carton label's allergen statement does not include fish.
The product, whose carton label lists ingredients such as salt, sodium glutamate, bonito, cornstarch, maltodextrin, water, flavored sodium nucleotide, glucose, and soybean protein powder, and notes soybean as an allergen, was recalled on July 9, 2026, with 109,600 units affected.
The recall was added to the FDA's Enforcement Report on August 4, 2026, and the product was distributed in California and New Jersey.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
Product details
"***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***"
- Lot code
- OA00822015
- Z2412426123
- Z2424526232
- Z2435226351
- Z2507827077
- Z2524927248
Recall details
- Company began the recall
- Sold in
- Company
- Pack'n Fresh LLCGrand Prairie, Texas
- Hazard
- Undeclared fish
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99460
- Recall number
- H-1194-2026
- Quantity recalled
- 109,600 units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
