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Lower risk Food recall · FDA · Published March 18, 2020

Aseltines Apple Cider Juice Recall: Patulin Over 50 ppb Risk

Aseltines recalls 1/2 and 1 gallon apple cider juice with patulin levels exceeding 50 ppb. Consumers should check UPCs 5169600064 and 5169600128 for affected products.

🇺🇸 FDA recall #F-0847-2020FoodAseltines ›
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Recalling firmAseltines573 Lamoreaux Dr Nw · Comstock Park, MI 49321-9204
✎ GovInfoNow plain-language explainer

What happened, in plain English

Aseltines is recalling 1/2-gallon and 1-gallon apple cider juice products due to patulin levels exceeding 50 ppb. This chemical, found in moldy apples, can cause health issues if consumed in high amounts. Read more at govinfonow.com/recall/15793-aseltines-apple-cider-juice-recall-patulin-over-50-ppb-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/15793-aseltines-apple-cider-juice-recall-patulin-over-50-ppb-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-0847-2020

Cite this page

“Aseltines Apple Cider Juice Recall: Patulin Over 50 ppb Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/15793-aseltines-apple-cider-juice-recall-patulin-over-50-ppb-risk. Based on FDA recall #F-0847-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0847-2020%22&limit=1).

Why it’s dangerous

Patulin is a mold byproduct that can form in apples when they're stored too long. High levels of patulin in juice can cause health issues, including gastrointestinal problems and potential long-term health risks. The product was tested to have patulin above the safe limit of 50 ppb.

Who’s affected

Consumers who purchased Aseltines 100% Apple Cider Juice with UPCs 5169600064 or 5169600128 between March 2020 and the sell-by date. Children and those with weakened immune systems may be at slightly higher risk due to patulin's potential health effects.

How to tell if you have this one

Check for UPC codes 5169600064 (1/2 gallon) or 5169600128 (1 gallon) on the product label. These items were sold until March 29, 2020.

  • Brand
    Aseltines
  • Product
    Aseltines 100% JUICE Apple Cider 1/2 gallon UPC 5169600064 and 1 gallon UPC 5169600128
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product UPC

    Look for UPC codes 5169600064 or 5169600128 on the juice container.

Where it went and when

Where it was distributed

Distributed in Illinois and Michigan.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew 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: 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: “Distributors in MI and IL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Michigan.

Recall timeline

FDA terminated this recall 15 days after the firm started it.

1. Firm started the recall: Mar 18, 202012. FDA classified it Class II: Mar 23, 202023. Published in FDA’s Enforcement Report: Apr 1, 202034. FDA terminated the recall: Apr 2, 202042020
  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-0847-2020 (March 18, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0847-2020 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