Wiers Farm Inc Recall: Listeria monocyotgenes contamination

🇺🇸 United States

1. July 11, 2024 - Recall initiated
2. August 14, 2024 - Reported by source
3. August 23, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1686-2024

Event ID

94998

Status

Terminated

Classification

Class I

Company

Wiers Farm Inc

Product description

Wiers Farm - Anaheim Peppers packaged into 1lb cartons - case size dependent on customer

Quantity

104 cases

Reason

Listeria monocyotgenes contamination

Recall initiation date

July 11, 2024

Report date

August 14, 2024

Classification date

Not published in this source record

Termination date

August 23, 2024

Distribution pattern

CT, DE, IL, IN, KY, ME, MD, MI, MO, NJ, NY, NC, OH, PA, RI, TN, VA, WV

UPC, lot, and code information

Lot No 240705, 240706, 240707, 240708, 240709, 240710, 240711, 240712

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

Other products recalled under this same event

This recall shares FDA event ID 94998 with 10 other product entries in Public Health Trace.

Responsible company: Wiers Farm Inc

Other recalls from Wiers Farm Inc

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
Connecticut	1
Delaware	1
Illinois	1
Indiana	1
Kentucky	1
Maine	1
Maryland	1
Michigan	1
Missouri	1
New Jersey	1
New York	1
North Carolina	1
Ohio	1
Pennsylvania	1
Rhode Island	1
Tennessee	1
Virginia	1
West Virginia	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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