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Lower risk Food recall · FDA · Published October 25, 2018

Valley Processing Apple Juice Concentrate Recall: High Arsenic Risk

Valley Processing recalls apple juice concentrates with high inorganic arsenic levels. Products distributed for non-fermentation use are affected. Consumers should check lot numbers for recall.

🇺🇸 FDA recall #F-0405-2019FoodValley Processing ›
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Recalling firmValley Processing Inc.108 Blaine Ave · Sunnyside, WA 98944-1458
✎ GovInfoNow plain-language explainer

What happened, in plain English

Valley Processing is recalling apple juice concentrates and organic apple juice concentrates that contain high levels of inorganic arsenic. These products were distributed for use other than fermentation (like alcohol or vinegar production). This recall is important because inorganic arsenic can cause serious health issues when consumed over time. Read more at govinfonow.com/recall/18220-valley-processing-apple-juice-concentrate-recall-high-arsenic-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/18220-valley-processing-apple-juice-concentrate-recall-high-arsenic-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-0405-2019

Cite this page

“Valley Processing Apple Juice Concentrate Recall: High Arsenic Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/18220-valley-processing-apple-juice-concentrate-recall-high-arsenic-risk. Based on FDA recall #F-0405-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0405-2019%22&limit=1).

Why it’s dangerous

The apple juice concentrates contain high levels of inorganic arsenic, a toxic chemical that can cause health problems when consumed over time. The hazard is specific to products distributed for non-fermentation uses, meaning they were intended for alcohol or vinegar production rather than direct food consumption.

Who’s affected

People who purchased or use Valley Processing apple juice concentrates for non-fermentation purposes, such as making alcohol or vinegar, are affected. Those who use the products for food purposes are not included in this recall.

How to tell if you have this one

Check for lot numbers 070617-C5, 070617-C6, or 062217-C5 (organic) on 52-gallon drums, 5-gallon pails, 4-gallon pails, and 260-gallon totes. Products distributed for non-fermentation uses (like alcohol or vinegar) are affected.

  • Brand
    Valley Processing
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Numbers

    Look for lot numbers 070617-C5, 070617-C6, or 062217-C5 (organic) on the product packaging.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Wholesale to customers nationwide and internationally (Canada and Korea)” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 2.4 years after the firm started it.

1. Firm started the recall: Oct 25, 201812. FDA classified it Class II: Nov 7, 201823. Published in FDA’s Enforcement Report: Nov 14, 201834. FDA terminated the recall: Mar 2, 2021420182021
  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-0405-2019 (October 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0405-2019 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.
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