Food recall: Ottogi Rice Cake Soup, 6.4oz. UPC 6 45175 89093 52; Item Number 29409101; Ingredients: 1. Rice Cake: Rice Water, Salt…
Class I FDA enforcement event 78976. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Firm determined that their Rice Cake Soup has undeclared milk in the form of sodium caseinate.
Class I, in the words of FDA
a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death
Ottogi America Inc started this food recall on 16 Jan 2018. The firm address in the FDA record is in Gardena, CA. FDA put the recall in Class I. FDA event 78976 has 1 product record. The first FDA enforcement report date is 7 Feb 2018. The record gives the status Terminated, with the termination date 11 May 2018.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Il, TX, NJ, CA, GA, AZ, HI, CO, OR, UT, WA, NV,
Recalling firm
Ottogi America Inc, Gardena, CA.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
1 product record in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0697-2018 | Ottogi Rice Cake Soup, 6.4oz. UPC 6 45175 89093 52; Item Number 29409101; Ingredients: 1. Rice Cake: Rice Water, Salt, Spirits; 2. Liquid Soup: Beef Bone Extract, Prim/starch syrup, coconut oil, sodium Caseinate, Water, Salt, Maltodextrin, Garlic, Chicken Extract Powder. (USA) Sugar, Black Pepper, monosodium… | 10,800 units or 900 cases | Class I | Terminated | 7 Feb 2018 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class I: The highest of the three FDA recall classes.
The event in context
- Food events that started in 2018
- 578
- Share of these events in Class I
- 34%
- Product records in this event
- 1Median of the firm: 2
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 15 Jan 2019 | Ottogi Ramen Sari (Extra Noodle) 3.88oz x 48ea Item #21101009 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ot | Food | Class I | 17 |
| 21 Nov 2018 | Ottogi Jin Ramen Spicy NET WT. 1lb 5.16oz, 600g (120gx5) 5PK Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ott | Food | Class I | 2 |
Official channels
- FDA enforcement report F-0697-2018The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 78976. https://recallregister.com/fda/i/78976/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Il, TX, NJ, CA, GA, AZ, HI, CO, OR, UT, WA, NV,
- What quantity of product is in FDA event 78976?
- The FDA record gives this quantity:
10,800 units or 900 cases
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2018 have the same class?
- 34% of the 578 food events that started in 2018 are in Class I.