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CriticalFDAfda-F-2381-2017UNDECLARED ALLERGEN

Master Carton is Labeled As: LOBSTER FLAVORED BALL DISTRIBUTED EXCLUSIVELY BY: H & C FOOD INC. BROOKLYN, NY 11237 KEEP FROZEN AT -18 C

⚠ 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
300
Recall Date
May 22, 2017
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2381-2017.

Product may contain undeclared egg,

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2381-2017.

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 H & C Food 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-2381-2017.

H & C Food Inc

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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H & C Food Inc Recall FAQ

H & C Food Inc is the subject of a seafood safety report: Master Carton is Labeled As: LOBSTER FLAVORED BALL DISTRIBUTED EXCLUSIVELY BY: H & C FOOD INC. BROOKLYN, NY 11237 KEEP FROZEN AT -18 C. The notice was published on May 22, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 300 units are potentially affected.