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High RiskFDAfda-F-1805-2017OTHER

KEEP REFIGERATED, DEEP BEET Blend 5 Gal, Ripe Liquid Produce

Category
Units Affected
80
Recall Date
February 24, 2017
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1805-2017.

Elevated patulin levels.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1805-2017.

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 Freshbev Llc 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-1805-2017.

Freshbev LLC

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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Freshbev Llc Recall FAQ

Freshbev Llc is the subject of a produce safety report: KEEP REFIGERATED, DEEP BEET Blend 5 Gal, Ripe Liquid Produce. The notice was published on February 24, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 80 units are potentially affected.