Negita Cracker- Shrimp
Reason Contains undeclared FD&C Yellow 6
Eishindo brand "CUP JELLY recall
Recalled by Hadson (Toko) Trading Co., Inc. · Maspeth, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product is a choking hazard.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Eishindo brand "CUP JELLY (MINI); NET WT. 28.2oz (800g); 50pcs; INGREDIENTS: WATER, HIGH FRUCTOSE SYRUP, APPLE JUIC, CARAGEENAN, CITRIC ACID, ARTIFICIAL FLAVOR, FD&C YELLOW NO. 5 TARTRAZINE, FD&C YELLOW NO. 6 SUNSET YELLOW FCF, FD&C BLUE NO.1 BRILLIANT BLUE FCF AND FD&C RED NO. 40; IMPORTED BY: HADSON TOKO TRADING CO., INC; PRODUCT OF JAPAN; WARNING PLEASE CHEW THOROUGHLY BEFORE SWALLOWING OR CUT THE JELLY INTO SMALL BITE SIZE PEICES BEFORE EATING; DO NOT EAT WHILE PERFORMING PHYSICAL ACTIVITIES, NOT RECOMMENDED FOR CHILDREN UNDER 5 YEARS OLD AND THE ELDERLY WITHOUT STRICT SUPERVISION, DO NOT FREEZE
Quantity: 625 cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
All codes.
Where it was sold
Colorado Connecticut Florida Georgia Illinois Indiana Kansas Massachusetts Maryland Michigan Missouri North Carolina North Dakota New Jersey Ohio Pennsylvania Rhode Island Tennessee Texas Virginia West Virginia
FDA's distribution note: N Y, NJ, CT, MA, OH, FL, IL, MI, PA, RI, NC, MD, WV, KS, TN, MO, TX, GA, CO, VA, IN, ND
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Hadson (Toko) Trading Co., Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 14, 2020
- In FDA report of
- Nov 4, 2020
- Terminated
- Aug 19, 2021
- FDA recall number
- F-0072-2021 · event 86603
- Official record
- FDA enforcement report search