Grand Supercenter Inc. FDA recall records
The FDA has published 7 food recall enforcement records naming Grand Supercenter Inc. between 2012 and 2017, covering 2 separate recall events. The firm is recorded in New Jersey. Data last updated 2 September 2026.

- Records of 29,386
- 7
- Share of all recalls
- 0%
- Class I of 7
- 0
- Reported between
- 2012 to 2017
What these records are
Every record on this page was published by the FDA in the openFDA food enforcement database. 7 records cover 2 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.
0 of these records are Class I, 7 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.
What was recalled for
A single record can name more than one hazard, so these counts overlap.
By year
Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.
Where the recalling firms are
The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.
Most recently reported
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2017-10-11 | HAIOREUM, RICE POP SNACK, KOREAN STYLE SNACK 0.41 LBS (190 G) | Grand Supercenter Inc. | The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen. | Class II |
| 2017-10-11 | HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G), Pumpkin | Grand Supercenter Inc. | The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen. | Class II |
| 2017-10-11 | HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G), Matcha (Green Tea) | Grand Supercenter Inc. | The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen. | Class II |
| 2017-10-11 | HAIOREUM, RICE PANCAKE, KOREAN STYLE SNACK 5.29 OZ (150 G), Sweet Potato | Grand Supercenter Inc. | The firm, Grand Supercenter Inc., was notified by USFDA NY District Office that they received a report from a consumer in which there was an allergy reaction after the person consumed Haioreum Rice Pop Snack. The firm Grand Supercenter Inc. has decided to recall the product involved in this incident due to Undeclared Wheat allergen. | Class II |
| 2012-07-04 | Frozen Seasoned and Cooked Clam Meat with Hot Pepper (Item #33229120) (5kg X 2). | Grand Supercenter Inc. | Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and products containing KMS as ingredients are adulterated under Section 40(a)(4) in that they were prepared and held under insanitary conditions, whereby they may have become contaminated with filth or whereby they may have been rend | Class II |
| 2012-07-04 | Frozen Oysters: 1) I.Q.F. 2 LB/12 Frozen Oyster (Permit #NJ36RS) - Item #33200115.; I.Q.F. (T-Size) 8 oz/40 Frozen Oyster (Permit #NJ36RS) - Item #33200116; BLOCK 1 LB/30 Frozen Oyster (Permit #NJ36RS) - Item #33200117. I.Q.F. (S Size) 5 LB/6 Frozen Oyster (Permit #NJ36RS) - Item #33200118. 2) Oyster 30/1 LB Frozen Oyster (Permit # NJ36RS) 3) IQF 2LB/12 Frozen Oyster and 8OZ/40 Frozen Oyster (Permit # NJ36RS). | Grand Supercenter Inc. | Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and products containing KMS as ingredients are adulterated under Section 40(a)(4) in that they were prepared and held under insanitary conditions, whereby they may have become contaminated with filth or whereby they may have been rend | Class II |
| 2012-07-04 | Oyster 8 oz. x 40 Korea "Farm Raised" | Grand Supercenter Inc. | Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and products containing KMS as ingredients are adulterated under Section 40(a)(4) in that they were prepared and held under insanitary conditions, whereby they may have become contaminated with filth or whereby they may have been rend | Class II |
Questions
- How many FDA recalls has Grand Supercenter Inc. had?
- The FDA has published 7 food recall enforcement records naming Grand Supercenter Inc. between 2012 and 2017. Those records cover 2 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
- Does a high recall count mean a firm is unsafe?
- Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.
A recall is the end of an evidence trail that either existed or did not. 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.