Townsend Farms Inc Recall: Kirkland Signature Three Berry Blend product is recalled due to potential contamination with Hepatitis A virus.

🇺🇸 United States

1. June 7, 2019 - Recall initiated
2. August 28, 2019 - Reported by source
3. September 28, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2077-2019

Event ID

83098

Status

Terminated

Classification

Class I

Company

Townsend Farms Inc

Product description

Kirkland Signature Three Berry Blend product, frozen, package in a plastic bag. Net wt. 4 lbs. UPC 0 96619 10105 4. The product label is read in parts: "*** KIRKLAND Signature *** Three Berry Blend *** Raspberries***Blueberries***Blackberries*** PRODUCT OF USA *** Distributed by: Costco Wholesale Corporation ***".

Quantity

6,921 cases (total 69,210 lbs.)

Reason

Kirkland Signature Three Berry Blend product is recalled due to potential contamination with Hepatitis A virus.

Recall initiation date

June 7, 2019

Report date

August 28, 2019

Classification date

Not published in this source record

Termination date

September 28, 2020

Distribution pattern

Distributed in Arizona, California, Hawaii, New Mexico, and Nevada

UPC, lot, and code information

Following Best By dates codes with vendor #63720: FEB1620,(A),(B),(C),(D),(E),(F),(G), or (H); FEB1820,(A),(B),(C),or (D); FEB2920,(A),(B),(C),or (D); MAR0120,(A),(B),(C),or (D); APR1920,(B),(C), or (D); APR2020(A),(B),(C),(D),(E), or (F); APR2720(A),(B),(C),(D),(E),(F),(G), or (H); APR2820(A),(B),(C),(D),(E),(F),(G), or (H); MAY0220(A),(B),(C),(D),(E),(F),(G), or (H); MAY0420 (H).

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

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: Townsend Farms Inc

Other recalls from Townsend Farms Inc

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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