CLASS I Food recall · Reported 12 Sep 2024 · USDA FSIS

Wiener Products recalled by Dearborn Sausage

Dearborn Sausage is recalling Array. The recall was initiated on 12 Sep 2024 and the FDA has classified it as Class I.

Recall details

Recall number
FSIS-026-2024
Recalling firm
Dearborn Sausage
Classification
Class I
Status
Completed
Recall initiated
12 Sep 2024
Reported
12 Sep 2024
USDA notice type
Closed Recall
Reason category
Undeclared Soy
Product category
Sausage

Timeline

12 Sep 2024Recall initiated by company
12 Sep 2024Published in enforcement report+0 days

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

Reason for recall

Array. WASHINGTON, Sept. 12, 2024 – Dearborn Sausage Company, Inc., a Dearborn, Mich. establishment, is recalling approximately 1,944 pounds of ready-to-eat (RTE) wiener products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The labels of the two products implicated in the recall were inadvertently swapped resulting in soy, a known allergen, and pork not being declared on the product labels.  The RTE wiener items were produced August 7, 2024. The following products are subject to recall [view labels]: 2-lb. vacuum-sealed packages of “BROOKSIDE BRAND FULLY COOKED NATURAL CASING BEEF WIENERS” that may contain undeclared pork with lot code A0122024 and sell by date 11/05/2024. 2-lb. vacuum-sealed packages of “BROOKSIDE BRAND NATURAL CASING FULLY COOKED WIENERS” that may contain undeclared soy with lot code A0322024 and sell by date 11/05/2024. The products subject to recall bear establishment number “EST. 10002” inside the USDA mark of inspection. These items were shipped to retail locations in Ohio. The problem was discovered when the establishment received a complaint from a retailer that the products they received may have been incorrectly labeled. The establishment determined that they inadvertently mislabeled beef wiener products as beef and pork wiener products and vice versa. The products labeled as beef and pork wiener products actually contain beef wiener products that contain soy;

Product as listed by the USDA

Array

Where it was distributed

Array

Questions about this recall

Why was it recalled?

Array. WASHINGTON, Sept. 12, 2024 – Dearborn Sausage Company, Inc., a Dearborn, Mich. establishment, is recalling approximately 1,944 pounds of ready-to-eat (RTE) wiener products due to misbranding and undeclared allergens, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The labels of the two products implicated in the recall were inadvertently swapped resulting in soy, a known allergen, and pork not being declared on the product labels.  The RTE wiener items were produced August 7, 2024. The following products are subject to recall [view labels]: 2-lb. vacuum-sealed packages of “BROOKSIDE BRAND FULLY COOKED NATURAL CASING BEEF WIENERS” that may contain undeclared pork with lot code A0122024 and sell by date 11/05/2024. 2-lb. vacuum-sealed packages of “BROOKSIDE BRAND NATURAL CASING FULLY COOKED WIENERS” that may contain undeclared soy with lot code A0322024 and sell by date 11/05/2024. The products subject to recall bear establishment number “EST. 10002” inside the USDA mark of inspection. These items were shipped to retail locations in Ohio. The problem was discovered when the establishment received a complaint from a retailer that the products they received may have been incorrectly labeled. The establishment determined that they inadvertently mislabeled beef wiener products as beef and pork wiener products and vice versa. The products labeled as beef and pork wiener products actually contain beef wiener products that contain soy;

Where was it sold?

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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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official USDA FSIS notice · Source record retrieved 26 Sep 2026. USDA data is public domain. This page reports the record and gives no medical advice.

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