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Lower risk Food recall · FDA · Published June 28, 2019

Valley Processing Single Strength Apple Juice Recall: Patulin Over 50 ppb

Valley Processing recalls single strength apple juice with patulin levels exceeding 50 ppb. This may pose health risks. Consumers should check lot numbers and contact Valley Processing for details.

🇺🇸 FDA recall #F-1581-2019FoodValley Processing ›
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Contact the company

Recalling firmValley Processing, Inc.108 Blaine Ave · Sunnyside, WA 98944-1458
✎ GovInfoNow plain-language explainer

What happened, in plain English

Valley Processing recalled single strength apple juice shipped in a 5700-gallon tanker due to patulin levels above 50 ppb. This chemical can be harmful to health, especially for children and those with sensitive systems. Read more at govinfonow.com/recall/17008-valley-processing-single-strength-apple-juice-recall-patulin-over-50.

Source Summary by GovInfoNow · govinfonow.com/recall/17008-valley-processing-single-strength-apple-juice-recall-patulin-over-50 · Updated October 5, 2026 · FDA enforcement record: FDA #F-1581-2019

Cite this page

“Valley Processing Single Strength Apple Juice Recall: Patulin Over 50 ppb.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17008-valley-processing-single-strength-apple-juice-recall-patulin-over-50. Based on FDA recall #F-1581-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1581-2019%22&limit=1).

Why it’s dangerous

Patulin is a natural compound that can form in apples and apple products. Levels above 50 ppb in juice may cause health issues, particularly for children and those with sensitive immune systems.

Who’s affected

Anyone who purchased Valley Processing single strength apple juice with lot number 083018-J5. Children and individuals with compromised immune systems are at slightly higher risk due to patulin's potential health effects.

How to tell if you have this one

Check for the lot number 083018-J5 on the label. The product was shipped in a 5700-gallon tanker with the label reading: '***SINGLE STRENGTH APPLE JUICE ***VALLEY PROCESSING INC. SUNNYSIDE, WA'.

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

What to do — step by step

  1. Check Product Label

    Look for the lot number 083018-J5 on the label of the single strength apple juice.

Where it went and when

Where it was distributed

Distributed in California.

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: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: 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 CA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

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

1. Firm started the recall: Jun 28, 201912. FDA classified it Class II: Jul 17, 201923. FDA terminated the recall: Jul 22, 201934. Published in FDA’s Enforcement Report: Jul 24, 201942019
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-1581-2019 (June 28, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1581-2019 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