CLASS II Food recall · Reported 23 Oct 2024 · FDA Enforcement Report

Lunds & Byerlys lone star dip recalled by Lund Food Holdings

Lund Food Holdings is recalling Lunds & Byerlys lone star dip, distributed in Minnesota. The recall was initiated on 27 Sep 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: 20240826, Use By: 10/15/24 Lot Code: 20240828, 20240829, Use By: 10/17/24

Quantity recalled756 units

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-0052-2025
FDA event ID: 95474
Recalling firm: Lund Food Holdings, Eden Prairie, MN
Brand: Lunds
Classification: Class II
Status: Terminated
Recall initiated: 27 Sep 2024
FDA classified: 16 Oct 2024
Reported: 23 Oct 2024
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Mold
Product category: Dips & Spreads

Timeline

27 Sep 2024	Recall initiated by company
16 Oct 2024	Classified by FDA	+19 days
23 Oct 2024	Published in enforcement report	+7 days

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

Reason for recall

Potential mold contamination.

Product as listed by the FDA

Lunds & Byerlys lone star dip. Net Wt 12 oz. (340.5g) UPC 0 18169-74197 9. Produced by Lunds & Byerlys, Edina, MN 55424.

Where it was distributed

Minnesota

Questions about this recall

Why was it recalled?

Potential mold contamination.

Which lots are affected?

Lot Code: 20240826, Use By: 10/15/24 Lot Code: 20240828, 20240829, Use By: 10/17/24

Where was it sold?

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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