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High RiskFDAfda-H-0679-2026UNDECLARED ALLERGEN

Negita Cracker- Shrimp 2.8oz

Category
Units Affected
142
Recall Date
April 16, 2026
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0679-2026.

Contains undeclared FD&C Yellow 6

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-H-0679-2026.

Recall ongoing. Follow firm instructions.

✅ 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 Hadson (toko) Trading Co. 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-H-0679-2026.

Hadson (Toko) Trading Co. Inc.

FDA

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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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Hadson (toko) Trading Co. Inc. Recall FAQ

Hadson (toko) Trading Co. Inc. is the subject of a seafood safety report: Negita Cracker- Shrimp 2.8oz. The notice was published on April 16, 2026 by the U.S. Food and Drug Administration (FDA). Approximately 142 units are potentially affected.