RecallHawk
Class II Recall

Ito-Shoten Seasoned Mushroom 200g/7.06 oz. Product of Japan Distributed by Mitsuwa Corporation Torrance, CA 90501

Mitsuwa Corporation

Summary

The FDA issued a Class II for Ito-Shoten Seasoned Mushroom 200g/7.06 oz. Product of Japan Distributed by Mitsu by Mitsuwa Corporation. Reason: Foreign manufacturer of recalled product listed on IA #99-37 due to having no filed scheduled process..

Details

Source

Food Recall

External ID

F-0854-2024

Action Date

2024-02-14

Status

Terminated

Category

food

Product Description

Ito-Shoten Seasoned Mushroom 200g/7.06 oz. Product of Japan Distributed by Mitsuwa Corporation Torrance, CA 90501

Lot/Code Info: Batch 1. 09/09/22, 2. 01/23/23, and 3. 5/8/23

Quantity Affected: 450 cases

Reason for Recall

Foreign manufacturer of recalled product listed on IA #99-37 due to having no filed scheduled process.

Distribution

U.S. distribution to the following: CA, NJ, IL, TX, HI No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-12-13

Company

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 82 food recalls issued in the same week, part of 204 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 (Mitsuwa Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Mitsuwa Corporation have FDA actions?

This is the only FDA action we have on record for Mitsuwa Corporation in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0854-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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