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FoodRecallWatch
Class II, May Cause HarmF-0767-2019

Luckyberry Cold-Pressed Juice, Reset, Carrot, Apple, Ginger, Lemon, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS

Recalled by Luckyberry on Oct 30, 2018

Reviewed by FoodRecallWatch Editorial Team · Updated

Recall Summary

Luckyberry recalled Luckyberry Cold-Pressed Juice, Reset, Carrot, Apple, Ginger, Lemon, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Oct 30, 2018.

The FDA-published reason for this recall is: "The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations"

The product reached multiple states, recorded by the FDA as "To retailers in Lawrence, KS." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Lawrence, KS. The recall covers At least 4 bottles of product. The FDA has Terminated this recall (first reported Dec 26, 2018), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.

Reason for Recall

The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations

Product Description

Luckyberry Cold-Pressed Juice, Reset, Carrot, Apple, Ginger, Lemon, 16 FL OZ, Manufactured at Luckyberry Juice Caf¿, Lawrence, KS

Distribution

To retailers in Lawrence, KS.

What Should You Do?

  • 1.Check your kitchen for this product immediately.
  • 2.Do not consume the recalled product.
  • 3.Return the product to where you bought it for a full refund, or throw it away.
  • 4.If you have experienced any health issues, contact your healthcare provider.

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Terms Explained

Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.