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CriticalFDAfda-F-0417-2023UNDECLARED ALLERGEN

Chukar Cherries Cherry Bombs Bits 'n Pieces, item #21508, net wt. 12 oz. (340g). UPC 0 11261 21508 9. Product is packaged in clear plasti...

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
4,439
Recall Date
February 21, 2023
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0417-2023.

undeclared hazelnuts

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0417-2023.

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 Chukar Cherry Company Inc. 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-0417-2023.

Chukar Cherry Company Inc.

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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Chukar Cherry Company Inc. Recall FAQ

Chukar Cherry Company Inc. is the subject of a dairy safety report: Chukar Cherries Cherry Bombs Bits 'n Pieces, item #21508, net wt. 12 oz. (340g). UPC 0 11261 21508 9. Product is packaged in clear plasti.... The notice was published on February 21, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 4,439 units are potentially affected.