IQF Blueberry (30lbs. cases and 1400 lbs. totes)
Recalled by Oregon Potato Company LLC
Food recall
Oregon Potato Company LLC
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
Oregon Potato Company LLC has recalled IQF Blueberry (30lbs. cases and 1400 lbs. totes), according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on March 4, 2026 and was initiated on February 12, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers IQF Blueberry (30lbs. cases and 1400 lbs. totes), with approximately 55,689 lbs. affected. The company behind the recall is Oregon Potato Company LLC, based in Salem, OR. The FDA describes the product as: “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. W…”
Why was IQF Blueberry (30lbs. cases and 1400 lbs. totes) recalled?
According to the FDA, the stated reason for the recall is: “Listeria monocytogenes.” In plain terms, this recall relates to Listeria.
Listeria monocytogenes is a bacterium that can grow even at refrigerator temperatures, which makes it a particular concern in ready-to-eat foods. Health authorities warn that it can cause a serious infection called listeriosis, and that pregnant people, newborns, older adults, and those with weakened immune systems are especially vulnerable. This is why products potentially contaminated with Listeria are often recalled quickly.
What should you do?
If you think you may have bought IQF Blueberry (30lbs. cases and 1400 lbs. totes), compare it against the product description and identifying codes (Lot codes on 30 lbs. CASES: 2055 B2, 2065 B1, and 2065 B3. Lot codes on 1400 lbs. TOTES: 3305 A1 and 3305 B1. Expiration dates or best-by date: 2055 B2 expirat…) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Oregon Potato Company LLC or your local health authority.
About this recall
This recall was distributed in OR. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- March 4, 2026
- Recall started
- February 12, 2026
- Distributed in
- OR
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was IQF Blueberry (30lbs. cases and 1400 lbs. totes) recalled?+
According to the FDA: Listeria monocytogenes
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have IQF Blueberry (30lbs. cases and 1400 lbs. totes)?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0522-2026. Information last synced from the FDA on July 6, 2026.