Fresh Recalls

FDAClass II · Food · Recall H-1195-2026 · Recalled August 12, 2026

Big Way Hot Pot "Hot Pot Miso Paste" recall — Big Way Ca Inc

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
Big Way Hot Pot "Hot Pot Miso Paste"
Company / brand
Big Way Ca
Lot / serial / date codes
Item No. CKJ19067 Lot: 20251106Z1-1 Expiration: NOV/05/2026
Distribution
Product is exclusively distributed to two affiliated restaurants.
Agency product description and boundaries

Big Way Hot Pot "Hot Pot Miso Paste"; 1kg (35.3oz) unit package. Product is packaged in generic bulk packaging.

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: Undeclared milk from lactose.

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: Big Way Hot Pot "Hot Pot Miso Paste"

3. Open the official notice or contact

Official recall ID
H-1195-2026
Brand
Big Way Ca
Classification
Class II
Units affected
65 cases
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Pomona, CA, United States
Firm address
1648 W Orange Grove Ave, 91768-2153

Identifying details (verbatim from the notice)

Product codes / lots
Item No. CKJ19067 Lot: 20251106Z1-1 Expiration: NOV/05/2026
Distribution
Product is exclusively distributed to two affiliated restaurants.
Firm notified the public via
Telephone
FDA event ID
99513
Recall initiated
July 24, 2026
FDA classified
August 4, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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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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