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High RiskFDAfda-F-1102-2019OTHER

Nature's Nectar High Pulp Orange Juice, Never from Concentrate. Item # 420025. Pasteurized. Net 52 FL OZ (1.6 QT) 1.53L. Kosher. UPC...

Category
Units Affected
1,142
Recall Date
February 12, 2019
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1102-2019.

Product cannot be verified as having achieved a 5-log reduction per 21 CFR 120.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1102-2019.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Citrus Systems Inc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1102-2019.

Citrus Systems Inc

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Citrus Systems Inc Recall FAQ

Citrus Systems Inc is the subject of a beverages safety report: Nature's Nectar High Pulp Orange Juice, Never from Concentrate. Item # 420025. Pasteurized. Net 52 FL OZ (1.6 QT) 1.53L. Kosher. UPC.... The notice was published on February 12, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 1,142 units are potentially affected.