Kroger recalls Private Selection Frozen Triple Berry Medley (16 oz) due to possible Hepatitis A contamination. Consumers should check product dates and UPC codes for affected items.
“Kroger Private Selection Frozen Triple Berry Medley Recall: Hepatitis A Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17374-kroger-private-selection-frozen-triple-berry-medley-recall-hepatitis-a. Based on FDA recall #F-2075-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2075-2019%22&limit=1).
The Food and Drug Administration announced on June 7, 2019, that The Kroger Co voluntarily recalled PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY due to possible Hepatitis A contamination. The agency classified the recall as Class I.
How to tell if you have it
Brand: Kroger
Product: PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 16 oz
Best By: 06-19-20
UPC: 0001111087808
The hazard
The product may be contaminated with Hepatitis A. The FDA classified the recall as Class I, indicating a reasonable probability that the food will cause serious adverse health consequences or death.
Context
GovInfoNow's records show The Kroger Co has issued 32 other recalls since November 24, 2014. Recent brand recalls include a September 26, 2025, recall for Kroger Smoked Mozzarella Penne Salad due to Listeria risk and an October 11, 2024, recall for Kroger Home Chef Chicken Street Taco kits over Listeria contamination. Other recent recalls of similar products include a December 2, 2025, Mellace Wegmans Mixed Nuts recall for Salmonella risk and an April 27, 2026, Kroger HOMESTYLE Cheese Garlic Croutons recall for possible Salmonella risk.
How to tell if you have this one
Check for the product name 'Private Selection Frozen Triple Berry Medley', 16 oz size, and best-by date of 06-19-20 or earlier. The UPC code is 0001111087808.
Brand
Kroger
Category
Food
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Terminated
Distribution
Product was sent to nine distributors in the states of Indiana, Oregon, Washington, Arizona, Colorado, California and Utah. (The distribution center in Indiana further distributed the product to eight Kroger distribution centers.) Product was then distributed to 2301 retail locations in the states of Alabama, Alaska, Arizona, Arkansas, California, Colorado, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Mississippi, Missouri, Montana, Nebraska, Nevada, New Mexico, Ohio, Oregon, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, and Wyoming
Look for the best-by date on the package, which should be 06-19-20 or earlier.
Discard if Consumed
If you have eaten the product, discard any remaining items and contact a healthcare provider.
Where it went and when
Where it was distributed
Distributed in 30 states.
Listed by the agency
Not listed
FDA distribution: “Product was sent to nine distributors in the states of Indiana, Oregon, Washington, Arizona, Colorado, California and Utah. (The distribution center in Indiana further distributed the product to eight Kroger distribution centers.) Product…” States read from FDA’s own wording; “not listed” means the notice does not name it.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-2075-2019 (June 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2075-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.