Alpha Plant-Based Burrito - Philly 5.5 oz UPC 855099007023 Frozen
Summary
The FDA issued a Class II for Alpha Plant-Based Burrito - Philly 5.5 oz UPC 855099007023 Frozen by THE MISO BROTHERS INC. Reason: Frozen Breakfast sandwiches and breakfast burritos have been found to contain milk that is not declared on the label..
Details
Source
Food Recall
External ID
F-0330-2023
Action Date
2023-02-08
Status
Terminated
Category
food
Product Description
Alpha Plant-Based Burrito - Philly 5.5 oz UPC 855099007023 Frozen
Lot/Code Info: Lot # 072822PB, Expiration date: 7/28/2024 Lot # 101822PB, Expiration date: 10/18/2024 Lot # P2-22266, Expiration date: 9/23/2024
Quantity Affected: 31,092 units (total)
Reason for Recall
Frozen Breakfast sandwiches and breakfast burritos have been found to contain milk that is not declared on the label.
Distribution
Throughout US retail locations
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-21
Company
Glendale, 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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
THE MISO BROTHERS INC has 8 FDA actions in our database, including 8 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 (THE MISO BROTHERS INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does THE MISO BROTHERS INC have FDA actions?
THE MISO BROTHERS INC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0330-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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