RecallHawk
Class II Recall

" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vege

JFE FRANCHISING INC

Summary

The FDA issued a Class II for " Dumpling Vegetable 4.5 oz by JFE FRANCHISING INC. Reason: Foreign Object (Glass).

Details

Source

Food Recall

External ID

H-0638-2026

Action Date

2026-04-08

Status

Ongoing

Category

food

Product Description

" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953

Lot/Code Info: tba

Quantity Affected: Unknown

Reason for Recall

Foreign Object (Glass)

Distribution

AK, AR, AZ, CA, OR, CO, CT, DC, DE, ID, IN, KY, LA, MA, MD, ME, MI, MN, MS, MT, ND, NH, NJ, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, VT, WA, WI, WV, WY

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-05

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 59 food recalls issued in the same week, part of 204 food-related FDA actions this month.

JFE FRANCHISING INC has 20 FDA actions in our database, including 20 recalls.

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 (JFE FRANCHISING INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does JFE FRANCHISING INC have FDA actions?

JFE FRANCHISING INC has 20 FDA actions in our database, including 20 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0638-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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