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FDA recall, , High risk

Willamette Valley Fruit Company IQF Blueberry

Willamette Valley Fruit Company IQF Blueberry has Listeria contamination.

Recall ended Aug 27, 2026. Still check yours.

What happened

Oregon Potato Company LLC of Salem, Oregon recalled IQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA, due to Listeria monocytogenes. The product was packaged in a polyethylene bag within a corrugated 30lbs. case or in a polyethylene liner within a Gaylord 1400lbs. tote. The recall began on February 12, 2026.

The product was distributed in Michigan, Oregon, Washington, Wisconsin and in Canada. It was not sold to consumers from retail stores.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for food recalls:

  1. Return it to the store where you bought it, or throw it away.
  2. Don't give it to anyone else, such as a food bank, or to a pet.

Is yours affected?

Compare the details below with your product and check the FDA notice to confirm whether it is affected.

  1. IQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is

    Product details from the notice

    IQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is packaged in polyethylene bag within a corrugated 30lbs. case or packaged in polyethylene liner within a Gaylord 1400lbs. tote. Product was not sold to consumers from retail stores. Willamette Valley Fruit Company 2994 82nd Ave. NE Salem OR 97305

    Lot code
    • 1400
    • 3305

Recall details

Company began the recall
Sold in

Distributed in Michigan, Oregon, Washington, Wisconsin and in Canada.

Company
Oregon Potato Company LLCSalem, Oregon
Hazard
Listeria
Risk

High risk

There is a reasonable chance that eating it could cause serious health problems or death.

FDA Class I recall · How risk is rated

Event ID
98435
Recall number
H-0522-2026
Quantity recalled
55,689 lbs.

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. In FDA's weekly enforcement report

  4. Listed on Recall Canary

  5. Recall ended

  6. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 16, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)