CLASS II Food recall · Reported 18 Dec 2024 · FDA Enforcement Report

7-Eleven Chicken Salad Sandwich recalled by Northern Tier Bakery

Northern Tier Bakery is recalling 7-Eleven Chicken Salad Sandwich, distributed in Minnesota. The recall was initiated on 15 Nov 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesEnjoy Through 11-17-2024
Quantity recalled220 sandwiches

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0281-2025
FDA event ID
95802
Recalling firm
Northern Tier Bakery, Saint Paul Park, MN
Classification
Class II
Status
Terminated
Recall initiated
15 Nov 2024
FDA classified
12 Dec 2024
Reported
18 Dec 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Salad Kits

Timeline

15 Nov 2024Recall initiated by company
12 Dec 2024Classified by FDA+27 days
18 Dec 2024Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Tuna salad sandwiches were labeled as chicken salad sandwiches.

Product as listed by the FDA

7-Eleven Chicken Salad Sandwich, UPC 7 63913-79486 1. Net Wt. 7.0 oz (198g), Keep Refrigerated. Mfg By: Supermom's St. Paul Park, MN 55071

Where it was distributed

MN

Minnesota

Stores named: 7-Eleven

Questions about this recall

Why was it recalled?

Tuna salad sandwiches were labeled as chicken salad sandwiches.

Which lots are affected?

Enjoy Through 11-17-2024

Where was it sold?

MN

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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