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

Trail Bologna Meat Processing Kit recalled by Con Yeager Spice

Con Yeager Spice is recalling Trail Bologna Meat Processing Kit, distributed in 10 states. The recall was initiated on 11 Oct 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC code 797442404137. Lot # B241851006
Quantity recalled1844 Cases

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-0260-2025
FDA event ID
95571
Recalling firm
Con Yeager Spice, New Castle, PA
Classification
Class I
Status
Terminated
Recall initiated
11 Oct 2024
FDA classified
6 Dec 2024
Reported
18 Dec 2024
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Allergens
Product category
Ready Meals

Timeline

11 Oct 2024Recall initiated by company
6 Dec 2024Classified by FDA+56 days
18 Dec 2024Published in enforcement report+12 days

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

Reason for recall

Undeclared Allergen - Wheat and Soy

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Con Yeager Spice Company, Trail Bologna Meat Processing Kit, 17.88 Ounce pouches, UPC code 797442404137

Where it was distributed

IL,PA,KY,MD,MI,MN,NC,NY,OH,WV

IllinoisKentuckyMarylandMichiganMinnesotaNorth CarolinaNew YorkOhioPennsylvaniaWest Virginia

Questions about this recall

Why was it recalled?

Undeclared Allergen - Wheat and Soy

Which lots are affected?

UPC code 797442404137. Lot # B241851006

Where was it sold?

IL,PA,KY,MD,MI,MN,NC,NY,OH,WV

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 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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