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Lower risk Food recall · FDA · Published September 18, 2018

Oregon Heritage Farms Apple Cider Recall: Elevated Patulin Levels

Oregon Heritage Farms recalls 1-gallon apple cider due to elevated patulin levels. Patulin is a mold byproduct that can cause health issues. Consumers should check labels for UPC 8 53581 00202 0.

🇺🇸 FDA recall #F-0006-2019FoodOregon Heritage Farms ›
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Recalling firmOregon Heritage Developments Inc dba Oregon Heritage Farms21435 SW Scholls Ferry Rd · Beaverton, OR 97007-8736
✎ GovInfoNow plain-language explainer

What happened, in plain English

Oregon Heritage Farms is recalling 1-gallon apple cider products because they contain elevated levels of patulin, a mold byproduct that can cause health issues. This recall affects consumers who bought the product with the specific UPC code and label details mentioned. Read more at govinfonow.com/recall/18662-oregon-heritage-farms-apple-cider-recall-elevated-patulin-levels.

Source Summary by GovInfoNow · govinfonow.com/recall/18662-oregon-heritage-farms-apple-cider-recall-elevated-patulin-levels · Updated October 6, 2026 · FDA enforcement record: FDA #F-0006-2019

Cite this page

“Oregon Heritage Farms Apple Cider Recall: Elevated Patulin Levels.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18662-oregon-heritage-farms-apple-cider-recall-elevated-patulin-levels. Based on FDA recall #F-0006-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0006-2019%22&limit=1).

Why it’s dangerous

Patulin is a mold byproduct that can be present in apple cider. Elevated levels of patulin in this product may cause health issues, though the specific risks are not detailed in the recall notice.

Who’s affected

Consumers who purchased Oregon Heritage Farms Family Blend Apple Cider, 100% Juice in 1-gallon plastic containers with the UPC 8 53581 00202 0 are affected. Those who have the product are at risk of potential health issues from elevated patulin levels.

How to tell if you have this one

Check for the product label that says 'FAMILY BLEND Apple Cider 100% Juice Not from concentrate' and the UPC code 8 53581 00202 0. The product comes in a 1-gallon plastic container with lot codes like 227OHF18, 231OHF18, or 225OHF18.

  • Brand
    Oregon Heritage Farms
  • Product
    Oregon Heritage Farms Family Blend Apple Cider, 100% Juice, 1 gallon plastic container, UPC: 8 53581 00202 0. The label
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the label that states 'FAMILY BLEND Apple Cider 100% Juice Not from concentrate' and the UPC code 8 53581 00202 0.

Where it went and when

Where it was distributed

Distributed in Oregon.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew 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 OR.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon.

Recall timeline

FDA terminated this recall 24 days after the firm started it.

1. Firm started the recall: Sep 18, 201812. FDA classified it Class II: Oct 3, 201823. Published in FDA’s Enforcement Report: Oct 10, 201834. FDA terminated the recall: Oct 12, 201842018
  1. Firm started the recall
  2. FDA classified it Class II
  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 #F-0006-2019 (September 18, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0006-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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