RecallHawk
Class I Recall

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

CON YEAGER SPICE CO.

Summary

The FDA issued a Class I for Con Yeager Spice Company, Trail Bologna Meat Processing Kit, 17.88 Ounce pouches by CON YEAGER SPICE CO.. Reason: Undeclared Allergen - Wheat and Soy.

Details

Source

Food Recall

External ID

F-0260-2025

Action Date

2024-12-18

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: UPC code 797442404137. Lot # B241851006

Quantity Affected: 1844 Cases

Reason for Recall

Undeclared Allergen - Wheat and Soy

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2024-10-11

Company

CON YEAGER SPICE CO.

New Castle, PA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (CON YEAGER SPICE CO.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does CON YEAGER SPICE CO. have FDA actions?

This is the only FDA action we have on record for CON YEAGER SPICE CO. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0260-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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