JMH International, LLC Recall: Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.

🇺🇸 United States

1. October 21, 2020 - Recall initiated
2. December 16, 2020 - Reported by source
3. August 9, 2021 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0154-2021

Event ID

86645

Status

Terminated

Classification

Class III

Company

JMH International, LLC

Product description

Chef Myron's Premium Teriyaki Sauce, 64 FL OZ (1.89 L), Item # 400023118, 4 bottles/case

Quantity

4397 cases, 4 bottles/case

Reason

Product utilized a gluten-free claim but has as an ingredient a fermented soy sauce that is produced from wheat which was not processed to remove the gluten prior to fermentation.

Recall initiation date

October 21, 2020

Report date

December 16, 2020

Classification date

Not published in this source record

Termination date

August 9, 2021

Distribution pattern

Nationwide.

UPC, lot, and code information

Batch: J091690A; J091690B; J091690C; Expiration: 09/16/2021 Batch: J102890A; J102890B; J102890C; Expiration: 10/28/2021 Batch: J111190A; Expiration: 11/11/2021 Batch: J120990A; J120990B; J120990C; J120990D; Expiration: 12/09/2021 Batch: J021000A; J021000B; J021000C; Expiration: 02/10/2022 Batch: J031600A; J031600B; J031600C; J031600D; Expiration: 03/16/2022 Batch: J091500A; J091500B; J091500C; J091500D; Expiration: 09/15/2022

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 86645 with 7 other product entries in Public Health Trace.

Responsible company: JMH International, LLC

Other recalls from JMH International, LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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