House Of Thaller Inc Recall: The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.

🇺🇸 United States

1. June 17, 2017 - Recall initiated
2. October 4, 2017 - Reported by source
3. February 22, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-3362-2017

Event ID

77587

Status

Terminated

Classification

Class I

Company

House Of Thaller Inc

Product description

LANTANA White Bean HUMMUS NET WT. 10 oz (283g)

Quantity

39,942 cs/8/10 oz cups

Reason

The firm was notified by their ingredient supplier that the pine nuts may be contaminated with Listeria monocytogenes.

Recall initiation date

June 17, 2017

Report date

October 4, 2017

Classification date

Not published in this source record

Termination date

February 22, 2018

Distribution pattern

Product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NY, OH, OK, OR, PA, SC, TX, UT, VA, WA & WI. Product was also shipped to Canada.

UPC, lot, and code information

Expiration & Lot Codes: USE BY 19 JUN 2017A W1704129, USE BY 20 JUN 2017A W1704138, USE BY 22 JUN 2017A W1704161, USE BY 22 JUN 2017A W1704164, USE BY 22 JUN 2017A W1704165, USE BY 29 JUN 2017A W1704253, USE BY 29 JUN 2017A W1704254, USE BY 29 JUN 2017A W1704257, USE BY 30 JUN 2017A W1704274, USE BY 30 JUN 2017A W1704275, USE BY 04 JUL 2017A W1704346, USE BY 06 JUL 2017A W1704365, USE BY 06 JUL 2017A W1704366, USE BY 12 JUL 2017A W1704403, USE BY 12 JUL 2017A W1705004, USE BY 15 JUL 2017A W1705041, USE BY 15 JUL 2017A W1705044, USE BY 15 JUL 2017A W1705045, USE BY 18 JUL 2017A W1705088, USE BY 24 JUL 2017A W1705175, USE BY 24 JUL 2017A W1705176, USE BY 24 JUL 2017A W1705177, USE BY 26 JUL 2017A W1705199, USE BY 26 JUL 2017A W1705200, USE BY 27 JUL 2017A W1705201, USE BY 27 JUL 2017A W1705203, USE BY 27 JUL 2017A W1705207, USE BY 02 AUG 2017A W1705306, USE BY 02 AUG 2017A W1705307, USE BY 03 AUG 2017A W1705315, USE BY 03 AUG 2017A W1705316, USE BY 05 AUG 2017A W1705335, USE BY 05 AUG 2017A W1705336, USE BY 09 AUG 2017A W1705390, USE BY 10 AUG 2017A W1705401, USE BY 10 AUG 2017A W1705402 & USE BY 15 AUG 2017A W1706065.

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

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 77587 with 2 other product entries in Public Health Trace.

Responsible company: House Of Thaller Inc

Other recalls from House Of Thaller 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
Alabama	1
Arizona	1
California	1
Colorado	1
Connecticut	1
Florida	1
Georgia	1
Iowa	1
Idaho	1
Illinois	1
Indiana	1
Louisiana	1
Massachusetts	1
Maryland	1
Michigan	1
Minnesota	1
Missouri	1
North Carolina	1
North Dakota	1
Nebraska	1
New Jersey	1
New York	1
Ohio	1
Oklahoma	1
Oregon	1
Pennsylvania	1
South Carolina	1
Texas	1
Utah	1
Virginia	1
Washington	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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