Luckyberry Cold-Pressed Juice, Spicy Watermelon, Watermelon, Red Beet, Lime, Mint, Green Apple, Jalepeno, 16 FL OZ, Manufactured at Lucky...
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0773-2019.
The firm manufactured and distributed to retailers unpasteurized juice products in violation of 21 CFR 120 Juice HACCP regulations
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0773-2019.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Luckyberry or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-0773-2019.
Luckyberry
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.
Visit FDA.gov →📣 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.
Luckyberry Recall FAQ
Luckyberry is the subject of a beverages safety report: Luckyberry Cold-Pressed Juice, Spicy Watermelon, Watermelon, Red Beet, Lime, Mint, Green Apple, Jalepeno, 16 FL OZ, Manufactured at Lucky.... The notice was published on October 30, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 5 units are potentially affected.