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Class II: temporary or reversible health riskOngoing

Hadson (Toko) Trading Negita Cracker- Shrimp 2 Recall

Negita Cracker- Shrimp 2

Hadson (Toko) Trading Co. Inc. · Maspeth, NY

Risk level
Class II
Reported by FDA
May 6, 2026
Recall ID
H-0679-2026
Check your lot numberHow we source this data

Summary

Hadson (Toko) Trading recalled Negita Cracker- Shrimp 2 starting Apr 16, 2026. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report H-0679-2026 on May 6, 2026. Reason: Contains undeclared FD&C Yellow 6. Status: Ongoing.

Why it was recalled

Contains undeclared FD&C Yellow 6

Product description

Negita Cracker- Shrimp 2.8oz

Lot numbers, UPCs & expiration codes

UPC code: 4975934313310 Best by: 1/6/2027

Where it was sold

CT, GA, IL, MA, MD, NJ, NY, OH, PA, TX, UT, VA

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0679-2026
Classification
Class II
Status
Ongoing
Recall initiated
Apr 16, 2026
FDA report date
May 6, 2026
Quantity
142 units
Recall type
Voluntary: Firm initiated
Recalling firm
Hadson (Toko) Trading Co. Inc.

Original FDA data

Every field from FDA enforcement report H-0679-2026, exactly as published.

Show all FDA fields
City
Maspeth
State
NY
Status
Ongoing
Country
United States
Event ID
98780
Address
5718 Flushing Ave
Code information
UPC code: 4975934313310 Best by: 1/6/2027
Postal code
11378-3120
Report date
May 6, 2026
Product type
Food
Recall number
H-0679-2026
Classification
Class II
Recalling firm
Hadson (Toko) Trading Co. Inc.
Product quantity
142 units
Reason for recall
Contains undeclared FD&C Yellow 6
Voluntary / mandated
Voluntary: Firm initiated
Product description
Negita Cracker- Shrimp 2.8oz
Distribution pattern
CT, GA, IL, MA, MD, NJ, NY, OH, PA, TX, UT, VA
Recall initiation date
Apr 16, 2026
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Apr 28, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0679-2026, published May 6, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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