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CriticalFDAfda-F-2608-2017LISTERIA

POZZIBLE Goji Crisp; 20 g protein bar; Gluten Free; no Sugar added 2.25 oz. (64 g) YouBar Inc. Monterey Park, CA.

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Brand
Category
Units Affected
5,256
Recall Date
June 14, 2017
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2608-2017.

Firm was notified by supplier that cashew butter used in protein bars is under recall due to the potential of Listeria monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2608-2017.

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 Youbar 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-2608-2017.

YouBar

FDA

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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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Youbar Recall FAQ

Youbar is the subject of a food safety report: POZZIBLE Goji Crisp; 20 g protein bar; Gluten Free; no Sugar added 2.25 oz. (64 g) YouBar Inc. Monterey Park, CA.. The notice was published on June 14, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 5,256 units are potentially affected.