Fish Ball in Polybag 24/12oz., Item no. 20072, UPC Code 087703200722
Wang Globalnet recalled this product and the FDA reported the enforcement action on 20 December 2017 as Class I. The recall was initiated by the firm. Fish products contain undeclared egg and wheat.

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
- Fish Ball in Polybag 24/12oz., Item no. 20072, UPC Code 087703200722
- Reason for recall
- Fish products contain undeclared egg and wheat.
- Recalling firm
- Wang Globalnet
- Firm location
- Moonachie, New Jersey, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0489-2018
- Quantity
- 2 cases
- Distribution
- NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI, and NH
- Initiated
- 15 May 2017
- Reported by FDA
- 20 December 2017
- Terminated
- 23 January 2018
- Firm notified by
- Letter
- Product codes
- Expiration date: 03/15/2019
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 is one of 5 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 5 separate recalls, which almost every published figure does, overstates it by a factor of 5. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 5 of them.
- The recall ran for 8 months, from 15 May 2017 to termination on 23 January 2018. 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 11 states, and the FDA published the enforcement report 7 months after the firm began the recall.
- Recalls of fish or seafood run a median of 5 months, so this one was longer than usual for its category. Fish and fishery products are the one food category with their own HACCP regulation in the United States, 21 CFR part 123, because the hazards are species-specific: histamine in scombroid fish, ciguatera in reef fish, and Listeria in cold-smoked products.
Named in the distribution pattern: New York, New Jersey, Pennsylvania, Massachusetts, Maine, Virginia, Maryland, Delaware, Connecticut, Rhode Island, New Hampshire. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
The allergens named in this record: wheat, eggs, fish.
Filed under fish and seafood. A product can sit in more than one.
Other fish and seafood recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. 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 Wang Globalnet
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 6 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2025-09-24 | (Bulk) Oyster, Frozen, Raw Half Shell, 15lb(6.8kg) UPC: 10087703078342 Harvest Dates: Jan 03,2025, Jan 14,2025 | Wang Globalnet | Oyster product potentially contaminated with Norovirus | Class II |
| 2017-12-20 | Fish Tofu in Polybag 40/240g, Item no. 17185, UPC Code 087703171855 | Wang Globalnet | Fish products contain undeclared egg and wheat. | Class I |
| 2017-12-20 | Fish Cake in Polybag 10/2.2lbs, Item no. 12842 UPC Code 087703128422 | Wang Globalnet | Fish products contain undeclared egg and wheat. | Class I |
| 2017-12-20 | Fish Cake in Polybag 10/930g, Item no. 15731 UPC Code 087703157316 | Wang Globalnet | Fish products contain undeclared egg and wheat. | Class I |
| 2017-12-20 | Fish Cake in Polybag 20/1lb., Item no. 13125 UPC Code 087703131256 | Wang Globalnet | Fish products contain undeclared egg and wheat. | Class I |
| 2012-07-18 | Surasang Chanbada Frozen Oyster I.Q.F (8oz), 40pack/case | Wang Globalnet | Wang Globalnet is recalling Surasang Chanbada Frozen Oyster IQF because it has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health. | Class II |
All 7 records for Wang Globalnet
All 2017 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one 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.