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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Beverages

Golden Sunrise Cold Pressured Juice Recalled for Incorrect SKU Labeling

Agency Publication Date: March 22, 2024
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Summary

Pressery, LLC has recalled 684 bottles of its Golden Sunrise Cold Pressured Juice because they were labeled with the incorrect SKU (stock keeping unit) at the store level. The recall affects 11 fl. oz. bottles containing a blend of carrot, orange, pineapple, lemon, ginger, and turmeric. No illnesses or injuries have been reported in connection with this labeling error.

Risk

The product was found with an incorrect SKU label at retail locations, which can cause confusion during the checkout process and inventory tracking.

What You Should Do

  1. This recall affects 11 fl. oz. bottles of Golden Sunrise Cold Pressured Juice (Carrot, Orange, Pineapple, Lemon, Ginger & Turmeric) with UPC 099482530914 and a manufacture date (MFG) of 01/09/24 WGS.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact Pressery, LLC for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Golden Sunrise Cold Pressured Juice (11 fl. oz.)
Variants: Carrot, Orange, Pineapple, Lemon, Ginger & Turmeric
UPC Codes:
099482530914
Lot Numbers:
MFG on: 01/09/24 WGS

Quantity affected: 57 cases (12 bottles per case)

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94091
Status: Resolved
Manufacturer: Pressery, LLC
Sold By: retail stores
Manufactured In: United States
Units Affected: 57 cases: 12 bottles per case: 684 bottles
Distributed To: Nationwide

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.