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Food recall · FDA · Published February 12, 2019

Citrus Systems Inc recalls Nature's Nectar High Pulp Orange Juice, Never from Concentrate. Item # 420025. Pasteurized. Net 52 FL OZ (1.6 QT)

Citrus Systems recalls Nature's Nectar High Pulp Orange Juice (Item #420025) due to insufficient pasteurization, which may not meet safety standards for 5-log reduction. Consumers should check labels and contact the manufacturer for details.

🇺🇸 FDA recall #F-1102-2019FoodCitrus Systems ›
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Contact the company & request your remedy

Recalling firmCitrus Systems Inc415 11th Ave S · Hopkins, MN 55343-7843
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Citrus Systems is recalling Nature's Nectar High Pulp Orange Juice (Item #420025) because it may not have achieved the required 5-log reduction in pasteurization. This could mean the product is unsafe for consumption and might not meet federal safety standards. Read more at govinfonow.com/recall/17725-nature-s-nectar-orange-juice-recall-inadequate-pasteurization-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/17725-nature-s-nectar-orange-juice-recall-inadequate-pasteurization-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-1102-2019

Cite this page

“Nature's Nectar Orange Juice Recall: Inadequate Pasteurization Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17725-nature-s-nectar-orange-juice-recall-inadequate-pasteurization-risk. Based on FDA recall #F-1102-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1102-2019%22&limit=1).

Why it’s dangerous

The product may not have reached the required 5-log reduction in pasteurization as required by federal regulations. This could mean the juice is not safe to drink and might not meet safety standards for preventing harmful bacteria.

Who’s affected

All consumers who purchased Nature's Nectar High Pulp Orange Juice (Item #420025) from Aldi, Inc. in the U.S. are affected. Those with the product in their homes are most at risk.

How to tell if you have this one

Look for the product name 'Nature's Nectar High Pulp Orange Juice', item number 420025, and the UPC 4 099100 056907. The product was distributed by Aldi, Inc. starting April 12, 2019.

  • Brand
    Citrus Systems
  • Product
    Nature's Nectar High Pulp Orange Juice, Never from Concentrate. Item # 420025. Pasteurized. Net 52 FL OZ (1.6 QT)
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Verify the product name, item number, and UPC code to confirm if it matches the recalled items.

✎ GovInfoNow

Questions people ask

Is this product safe to drink?

The recall indicates the product may not have achieved the required 5-log reduction in pasteurization, which could mean it is unsafe for consumption.

How can I get a refund or replacement?

The recall record does not specify any remedy for refunds or replacements.

When was this product distributed?

The product was distributed by Aldi, Inc. starting April 12, 2019.

Take action

Contact Citrus Systems

We’ve drafted a message you can send Citrus Systems to request your refund or repair — edit it as you like.

Subject: Recall F-1102-2019 — Citrus Systems Nature's Nectar High Pulp Orange Juice, Never from Concentrate. Item # 420025. Paste

Hello,

I own a Nature's Nectar High Pulp Orange Juice, Never from Concentrate. Item # 420025. Pasteurized. Net 52 FL OZ (1.6 QT) that is covered by recall F-1102-2019 from Citrus Systems.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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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-1102-2019 (February 12, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1102-2019 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