Gluten Free Bean & Rice Burrito. 12 retail units per case. 5.5oz/retail unit. UPC code 042272003525. Frozen.
Summary
The FDA issued a Class II for Gluten Free Bean & Rice Burrito. 12 retail units per case. 5.5oz/retail unit. U by AMY'S KITCHEN INC.. Reason: Potential contamination with foreign objects..
Details
Source
Food Recall
External ID
H-0057-2026
Action Date
2025-10-22
Status
Terminated
Category
food
Product Description
Gluten Free Bean & Rice Burrito. 12 retail units per case. 5.5oz/retail unit. UPC code 042272003525. Frozen.
Lot/Code Info: Lot code: 30C1725, Expiration Date 03/2027
Quantity Affected: 3,238 cases/ 38,856 retail units
Reason for Recall
Potential contamination with foreign objects.
Distribution
Product distributed to the following states: CA, CO, CT, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, NY, OH, OK, PA, TX, VA, VT, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-02
Company
Petaluma, 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 75 food recalls issued in the same week, part of 204 food-related FDA actions this month.
AMY'S KITCHEN INC. has 3 FDA actions in our database, including 3 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 (AMY'S KITCHEN INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does AMY'S KITCHEN INC. have FDA actions?
AMY'S KITCHEN INC. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0057-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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