Fresh Recalls

FDAClass II · Food · Recall H-1194-2026 · Recalled August 12, 2026

"***Hondashi 0 recall — Pack'n Fresh LLC

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
"***Hondashi 0
Company / brand
Pack'n Fresh
Lot / serial / date codes
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
Distribution
NJ, CA
Agency product description and boundaries

"***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***"

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Allergen missing from contains statement: fish

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: "***Hondashi 0

3. Open the official notice or contact

Official recall ID
H-1194-2026
Brand
Pack'n Fresh
Classification
Class II
Units affected
109,600 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Grand Prairie, TX, United States
Firm address
1025 Avenue S Ste 150, 75050-1121

Identifying details (verbatim from the notice)

Product codes / lots
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
Distribution
NJ, CA
Firm notified the public via
E-Mail
FDA event ID
99460
Recall initiated
July 9, 2026
FDA classified
August 4, 2026
FDA report date
August 12, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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