Eishindo brand "CUP JELLY (MINI); NET WT. 28.2oz (800g); 50pcs; INGREDIENTS: WATER, HIGH…
Hadson (Toko) Trading Co., Inc. recalled this product and the FDA reported the enforcement action on 4 November 2020 as Class I. The recall was initiated by the firm. Product is a choking hazard.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- 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
- Reason for recall
- Product is a choking hazard.
- Recalling firm
- Hadson (Toko) Trading Co., Inc.
- Firm location
- Maspeth, New York, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0072-2021
- Quantity
- 625 cases
- Distribution
- N Y, NJ, CT, MA, OH, FL, IL, MI, PA, RI, NC, MD, WV, KS, TN, MO, TX, GA, CO, VA, IN, ND
- Initiated
- 14 October 2020
- Reported by FDA
- 4 November 2020
- Terminated
- 19 August 2021
- Firm notified by
- Press Release
- Product codes
- All codes.
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 10 months, from 14 October 2020 to termination on 19 August 2021. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 21 states, and the FDA published the enforcement report 3 weeks after the firm began the recall.
- Recalls of fresh produce run a median of 7 months, so this one was longer than usual for its category. Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
Named in the distribution pattern: New Jersey, Connecticut, Massachusetts, Ohio, Florida, Illinois, Michigan, Pennsylvania, Rhode Island, North Carolina, Maryland, West Virginia, Kansas, Tennessee, Missouri, Texas, Georgia, Colorado, Virginia, Indiana, North Dakota. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Filed under fresh produce and sauces, dips and condiments. A product can sit in more than one.
Other fresh produce recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Hadson (Toko) Trading Co., Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2026-05-06 | Negita Cracker- Shrimp 2.8oz | Hadson (Toko) Trading Co. Inc. | Contains undeclared FD&C Yellow 6 | Class II |
All 2020 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.