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

L & L Homemade Corn Salsa recalled by Levi A. Bontrager

Levi A. Bontrager is recalling L & L Homemade Corn Salsa, distributed in Illinois, Wisconsin. The recall was initiated on 1 Nov 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBB 4 17 26 printed on top of jars
Quantity recalled192 jars

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-0258-2025
FDA event ID
95782
Recalling firm
Levi A. Bontrager, Granton, WI
Classification
Class II
Status
Terminated
Recall initiated
1 Nov 2024
FDA classified
6 Dec 2024
Reported
18 Dec 2024
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Foreign Material
Product category
Dips & Spreads

Timeline

1 Nov 2024Recall initiated by company
6 Dec 2024Classified by FDA+35 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

Salsa had pH of 4.7.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

L & L Homemade Corn Salsa in 16 oz Glass jar. W1520 Starr Road, Granton, WI 54436

Where it was distributed

IL, WI

IllinoisWisconsin

Questions about this recall

Why was it recalled?

Salsa had pH of 4.7.

Which lots are affected?

BB 4 17 26 printed on top of jars

Where was it sold?

IL, WI

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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