Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life Box Net wt. 40oz (1.13kg) UPC: 85001598
Summary
The FDA issued a Class II for Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life B by Ittella International, LLC. Reason: A gluten free claim was inadvertently used on the lid of the container. However, the ingredient statement declares enriched wheat flour as an ingredie.
Details
Source
Food Recall
External ID
F-0992-2022
Action Date
2022-04-20
Status
Terminated
Category
food
Product Description
Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18-month shelf life Box Net wt. 40oz (1.13kg) UPC: 850015982569 Packed for: Tattooed Chef Paramount, CA 90723
Lot/Code Info: Lot code Best by Date 20A-325 5/20/2022 20P-325 5/20/2022 20A-327 5/22/2022 20P-327 5/22/2022 20A-328 5/23/2022 20P-328 5/23/2022 20A-329 5/24/2022 20P-329 5/24/2022 20A-335 5/30/2022 20P-335 5/30/2022 20A-336 6/1/2022 20P-336 6/1/2022 20A-337 6/2/2022 20P-337 6/2/2022 20A-338 6/3/2022 20P-338 6/3/2022 20A-356 6/21/2022 20P-356 6/21/2022 20A-357 6/22/2022 20P-357 6/22/2022 20A-358 6/23/2022 20P-358 6/23/2022
Quantity Affected: 12213 cases
Reason for Recall
A gluten free claim was inadvertently used on the lid of the container. However, the ingredient statement declares enriched wheat flour as an ingredient and the allergen information statement disclosed the presence of EGGS, WHEAT, MILK, SOY, COCONUT, in bolded text.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2021-01-04
Company
Paramount, CA
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 40 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 (Ittella International, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ittella International, LLC have FDA actions?
This is the only FDA action we have on record for Ittella International, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0992-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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