Food/Recall·openFDA/food

PS Seasoning & Spices, Inc. — Class I: Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). P

HighPublished May 27, 2026· AI-analyzed Jun 1, 2026View original FDA source
AI-generated regulatory interpretation. The four sections below are an analyst-style summary produced by an AI model from the original FDA source. Always verify against the source before any regulatory, clinical, or commercial decision.
What happened

PS Seasoning & Spices, Inc. initiated a Class I recall for its Ellsworth Sour Cream + Onion Seasoning (Part #180000113) in 25 lb containers. The recall was triggered after the firm discovered the product contained milk powder that had been recalled by a supplier for potential Salmonella contamination.

Who it affects

This recall affects food manufacturers and industrial users utilizing this specific seasoning blend in bulk quantities, as well as the quality and safety departments at PS Seasoning & Spices.

Why it matters

A Class I designation indicates a high risk of serious adverse health consequences or death. This situation highlights the operational risks of ingredient-driven recalls where a failure at the supplier level necessitates secondary recalls. Regulatory teams may view this as a potential gap in incoming material controls or supplier notification protocols.

Practical takeaway

QA teams should immediately verify if this specific lot of seasoning is in inventory or used in downstream processing. Supply chain managers should review supplier qualification programs, specifically addressing how primary ingredient recalls are communicated to secondary manufacturers.

FDA source material

Class I. Reason: Product was made with milk powder recalled by the supplier due to Salmonella contamination.. Product: Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). PS Seasoning & Spices 216 W Pleasant St Iron Ridge WI 53035. Firm: PS Seasoning & Spices, Inc. (Iron Ridge WI United States). Status: Ongoing.

Open in openFDA / FDA.gov
AI-generated interpretation. Always verify critical decisions against the original FDA source. Generated with google/gemini-3-flash-preview.