1P Original Smokehouse Unit for 300 lbs. of Meat, Part #: 180002964. Net Wt 15.10 lbs (6.85kg). PS Seasoning & Spices
Summary
The FDA issued a Class I for 1P Original Smokehouse Unit for 300 lbs. of Meat, Part #: 180002964. Net Wt 15. by PS Seasoning & Spices, Inc.. Reason: Product was made with milk powder recalled by the supplier due to Salmonella contamination..
Details
Source
Food Recall
External ID
H-0815-2026
Action Date
2026-05-27
Status
Ongoing
Category
food
Product Description
1P Original Smokehouse Unit for 300 lbs. of Meat, Part #: 180002964. Net Wt 15.10 lbs (6.85kg). PS Seasoning & Spices 216W Pleasant St Iron Ridge, WI 53035.
Lot/Code Info: Lot #: 2025-44770 Exp 05/27/2027
Quantity Affected: 5375.6 lbs
Reason for Recall
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-22
Company
Iron Ridge, WI
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 80 food recalls issued in the same week, part of 204 food-related FDA actions this month.
PS Seasoning & Spices, Inc. has 11 FDA actions in our database, including 11 recalls.
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 (PS Seasoning & Spices, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does PS Seasoning & Spices, Inc. have FDA actions?
PS Seasoning & Spices, Inc. has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0815-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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