Vegetable egg rolls packaged either 96 3oz per case or 120 2oz per case, Manufacturer T&R Enterprises St. Louis MO.
Summary
The FDA issued a Class II for Vegetable egg rolls packaged either 96 3oz per case or 120 2oz per case, Manufac by T & R Enterprises USA, Inc.. Reason: Products contain Yellow #5 but it is not declared on the label.
Details
Source
Food Recall
External ID
F-0868-2021
Action Date
2021-08-25
Status
Terminated
Category
food
Product Description
Vegetable egg rolls packaged either 96 3oz per case or 120 2oz per case, Manufacturer T&R Enterprises St. Louis MO.
Lot/Code Info: Best by October 2021 and earlier.
Quantity Affected: 630 cases
Reason for Recall
Products contain Yellow #5 but it is not declared on the label
Distribution
Distributed to restaurants in the St. Louis, MO area.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-07-01
Company
Saint Louis, MO
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 48 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 (T & R Enterprises USA, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does T & R Enterprises USA, Inc. have FDA actions?
This is the only FDA action we have on record for T & R Enterprises USA, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0868-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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