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Stop using now Food recall · FDA · Published February 12, 2026

Oregon Potato Company Recalls Frozen Blueberries Due to Listeria Risk

Oregon Potato Company recalls IQF frozen blueberries (30lb cases and 1400lb totes) with Listeria monocytogenes. Products sold in the US with specific lot codes and expiration dates.

🇺🇸 FDA recall #H-0522-2026FoodOregon Potato Company ›
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Contact the company

Recalling firmOregon Potato Company LLC2994 82nd Ave Ne · Salem, OR 97305-9552
✎ GovInfoNow plain-language explainer

Oregon Potato Company is recalling IQF frozen blueberries sold in 30-pound cases and 1400-pound totes due to a Listeria monocytogenes contamination risk. This bacteria can cause serious illness, so affected consumers should stop using the product immediately. Read more at govinfonow.com/recall/6743-oregon-potato-company-recalls-frozen-blueberries-due-to-listeria-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/6743-oregon-potato-company-recalls-frozen-blueberries-due-to-listeria-risk · Updated September 14, 2026 · Official notice: FDA #H-0522-2026

Cite this page

“Oregon Potato Company Recalls Frozen Blueberries Due to Listeria Risk.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/6743-oregon-potato-company-recalls-frozen-blueberries-due-to-listeria-risk. Based on FDA recall #H-0522-2026.

The FDA announced on Feb. 12, 2026, that Oregon Potato Company LLC is recalling IQF frozen blueberries due to a Listeria monocytogenes hazard. The voluntary Class I recall affects approximately 55,689 lbs of product distributed in Michigan, Oregon, Washington, Wisconsin, and Canada.

How to tell if you have it

  • Brand: Oregon Potato Company
  • Product: IQF frozen Blueberry
  • Packaging: 30lbs. cases (polyethylene bag within corrugated case) or 1400 lbs. totes (polyethylene liner within Gaylord tote)
  • Lot codes (30 lbs. CASES): 2055 B2, 2065 B1, and 2065 B3
  • Lot codes (1400 lbs. TOTES): 3305 A1 and 3305 B1
  • Expiration dates: 7/23/2027 (for lot 2055 B2), 7/24/2027 (for lots 2065 B1 and 2065 B3), 11/25/2027 (for lots 3305 A1 and 3305 B1)
  • Distribution: MI, OR, WA, WI and Canada

The hazard

The product is contaminated with Listeria monocytogenes. The FDA classified the recall as Class I, indicating a reasonable probability that the use of the product will cause serious adverse health consequences or death.

Context

GovInfoNow's records show other recent recalls of similar products include Willamette Valley Pie Company Recalls Blueberry Crumble Pies Due to Listeria Risk (2026-02-19) and Made Fresh Salads Blueberry Cream Cheese Recall: Listeria Contamination Risk (2026-02-19). A prior recall of Southern Rocklobster Australian Greenlip Abalone due to Listeria Contamination Risk occurred on 2025-12-24.

How to tell if you have this one

Check for 30-pound cases with lot codes 2055 B2, 2065 B1, or 2065 B3, or 1400-pound totes with lot codes 3305 A1 or 3305 B1. Products have expiration dates listed in the recall notice.

  • Brand
    Oregon Potato Company
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Product Now

    Immediately discard or return the recalled IQF frozen blueberries with the specified lot codes and expiration dates.

Where it went and when

Where it was distributed

Distributed in 4 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Distributed in MI, OR, WA, WI and in Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Michigan, Oregon, Washington, Wisconsin.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Feb 12, 202612. FDA classified it Class I: Feb 24, 202623. Published in FDA’s Enforcement Report: Mar 4, 202634. FDA terminated the recall: Aug 27, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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 #H-0522-2026 (February 12, 2026)
  • Plain-language summary written by qwen3:4b on September 14, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA