JUST Egg Inspired by Mexico Roasted Poblanos, Ancho Chilli Powder, Black Beans, Corn, Lime 4 Sous Vide Plant Egg Bites N
Summary
The FDA issued a Class II for JUST Egg Inspired by Mexico Roasted Poblanos, Ancho Chilli Powder, Black Beans, by Cuisine Solutions. Reason: Undeclared egg and milk.
Details
Source
Food Recall
External ID
F-0744-2021
Action Date
2021-07-07
Status
Terminated
Category
food
Product Description
JUST Egg Inspired by Mexico Roasted Poblanos, Ancho Chilli Powder, Black Beans, Corn, Lime 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402517, Expiration dates 3/3/2022, 3/29/2022, 3/10/2022, and 4/7/2022. 16 cartons per corrugated case, Carton GTIN 7 05044 02517 9 Case Bar Code 10 7054 402 5176
Lot/Code Info: 82543, 82784, and 83368
Quantity Affected: 4339 cases
Reason for Recall
Undeclared egg and milk
Distribution
Distributed nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2021-06-18
Company
Sterling, VA
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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Cuisine Solutions has 4 FDA actions in our database, including 4 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 (Cuisine Solutions) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cuisine Solutions have FDA actions?
Cuisine Solutions has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0744-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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