FindMyRecallSubscribe
Class III: unlikely to cause harmTerminated

Hikari Enjuku Koji Miso Mutenka Recall

Hikari Enjuku Koji Miso Mutenka

Hikari Miso International, Inc. · Torrance, CA

Risk level
Class III
Reported by FDA
Mar 20, 2019
Recall ID
F-1189-2019
Check your lot numberHow we source this data

Summary

Hikari Miso International recalled Hikari Enjuku Koji Miso Mutenka starting Feb 1, 2019. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1189-2019 on Mar 20, 2019. Reason: Miso product manufactured in Japan was distributed in US with no English labeling and therefore soy beans not properly declared on label as an allergen. Status: Terminated.

Why it was recalled

Miso product manufactured in Japan was distributed in US with no English labeling and therefore soy beans not properly declared on label as an allergen.

Product description

Hikari Enjuku Koji Miso Mutenka; 26.6 oz. plastic tub with lid. UPC 4 905663 003007

Lot numbers, UPCs & expiration codes

Best Before 28.OCT. 2019

Where it was sold

One distributor in CA only

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1189-2019
Classification
Class III
Status
Terminated
Recall initiated
Feb 1, 2019
FDA report date
Mar 20, 2019
Quantity
224 cases ( 8 tubs per case)
Recall type
Voluntary: Firm initiated
Recalling firm
Hikari Miso International, Inc.

Original FDA data

Every field from FDA enforcement report F-1189-2019, exactly as published.

Show all FDA fields
City
Torrance
State
CA
Status
Terminated
Country
United States
Event ID
82306
Address
357 Van Ness Way Ste 210
Code information
Best Before 28.OCT. 2019
Postal code
90501-1483
Report date
Mar 20, 2019
Product type
Food
Recall number
F-1189-2019
Classification
Class III
Recalling firm
Hikari Miso International, Inc.
Product quantity
224 cases ( 8 tubs per case)
Termination date
Jun 7, 2019
Reason for recall
Miso product manufactured in Japan was distributed in US with no English labeling and therefore soy beans not properly declared on label as an allergen.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Hikari Enjuku Koji Miso Mutenka; 26.6 oz. plastic tub with lid. UPC 4 905663 003007
Distribution pattern
One distributor in CA only
Recall initiation date
Feb 1, 2019
Initial firm notification
Letter
Center classification date
Mar 25, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1189-2019, published Mar 20, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls