RecallHawk
Class II Recall

"***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch, pouches packed in brown paperboard cartons (6

Pack'n Fresh LLC

Summary

The FDA issued a Class II for "***Hondashi 0.25oz***" seasoning packed in silver plastic/metallic pouch, pouch by Pack'n Fresh LLC. Reason: Allergen missing from contains statement: fish.

Details

Source

Food Recall

External ID

H-1194-2026

Action Date

2026-08-12

Status

Ongoing

Category

food

Product Description

"***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 Info: 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

Quantity Affected: 109,600 units

Reason for Recall

Allergen missing from contains statement: fish

Distribution

NJ, CA

Type: Voluntary: Firm initiated

Recall Initiated: 2026-07-09

Company

Pack'n Fresh LLC

Grand Prairie, TX

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 36 food recalls issued in the same week, part of 73 food-related FDA actions this month.

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 (Pack'n Fresh LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Pack'n Fresh LLC have FDA actions?

This is the only FDA action we have on record for Pack'n Fresh LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1194-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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