Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. D
Summary
The FDA issued a Class II for Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 1 by Target Corporation. Reason: Undeclared allergens (sesame and soy).
Details
Source
Food Recall
External ID
H-0761-2026
Action Date
2026-05-13
Status
Ongoing
Category
food
Product Description
Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. DPCI # 878-02-0227. UPC (01) 00250086000009 (3922) 00999. Distributed by SuperTarget Mpls, MN 55403.
Lot/Code Info: Use or Freeze By: 4/15/26 through 4/27/26
Quantity Affected: 558 units
Reason for Recall
Undeclared allergens (sesame and soy)
Distribution
AL, AZ, CA, CO, FL, GA, IA, IL, IN, KS, LA, MN, MO, NC, ND, NE, OK, TN, TX, UT, VA, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-24
Company
Minneapolis, MN
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 93 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Target Corporation 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 (Target Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Target Corporation have FDA actions?
Target Corporation 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-0761-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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