RecallHawk
Class II Recall

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

Big Way Ca Inc

Summary

The FDA issued a Class II for Big Way Hot Pot "Hot Pot Miso Paste"; 1kg (35.3oz) unit package. Product is pack by Big Way Ca Inc. Reason: Undeclared milk from lactose..

Details

Source

Food Recall

External ID

H-1195-2026

Action Date

2026-08-12

Status

Ongoing

Category

food

Product Description

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

Lot/Code Info: Item No. CKJ19067 Lot: 20251106Z1-1 Expiration: NOV/05/2026

Quantity Affected: 65 cases

Reason for Recall

Undeclared milk from lactose.

Distribution

Product is exclusively distributed to two affiliated restaurants.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-07-24

Company

Big Way Ca Inc

Pomona, CA

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 (Big Way Ca Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Big Way Ca Inc have FDA actions?

This is the only FDA action we have on record for Big Way Ca Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1195-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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