Class ITerminated in FDA datasetRecall initiated Jun 7, 2019

Kirkland Signature Three Berry Blend product, frozen, package in a plastic bag. Net wt. 4 lbs.

Recalling firm: Townsend Farms Inc

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 28, 2020.

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ProductKirkland 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 ***".
Package size4 lbs
UPC096619101054

FDA 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).

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Full FDA record and distribution details

Original 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 ***".

Extracted codes and context

TypeCode / valueContext
UPC096619101054hree 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***B

Original FDA recall reason

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

Recall details

Recall number
F-2077-2019
Event ID
83098
FDA status
Terminated
Initiated
Jun 7, 2019
Reported
Aug 28, 2019
Classified
Aug 20, 2019
Terminated
Sep 28, 2020
Quantity
6,921 cases (total 69,210 lbs.)
Location
Fairview, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

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

FDA source record · F-2077-2019

Data updated September 16, 2026. View official FDA data ↗

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