Shearers Foods, Llc Recall: Milk allergen was not declared on the labeling of the product.

🇺🇸 United States

1. May 29, 2018 - Recall initiated
2. June 20, 2018 - Reported by source
3. February 14, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1541-2018

Event ID

80191

Status

Terminated

Classification

Class I

Company

Shearers Foods, Llc

Product description

Meijer DILL PICKLE FLAVORED CLASSIC CRUNCH POTATO CHIPS***UPC 719283594365***LOT CODE***

Quantity

2273 Cases with 11 bags (9.5 oz) per case

Reason

Milk allergen was not declared on the labeling of the product.

Recall initiation date

May 29, 2018

Report date

June 20, 2018

Classification date

Not published in this source record

Termination date

February 14, 2019

Distribution pattern

Products were distributed in Michigan only to their distributor. However, products were eventually distributed to OH, MI, IN, IL, KY and WI.

UPC, lot, and code information

UPC 719283594365; UPC: 719283594365 Lot Code 04110831 Sell By 07/16/18 Lot Code 04210831 Sell By 07/16/18 Lot Code 04311632 Sell By 07/16/18 Lot Code 04111732 Sell By 07/16/18 Lot Code 04312430 Sell By 07/23/18 Lot Code 04213135 Sell By 07/30/18 Lot Code 04114434 Sell By 08/13/18

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Shearers Foods, Llc

Other recalls from Shearers Foods, Llc

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Ohio	1
Michigan	1
Indiana	1
Illinois	1
Kentucky	1
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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