Food recall: You-ka Fresh Ramune Net Wt. 3.87oz (110g), Item No. 23925, 20 packs/case
Class II FDA enforcement event 75788. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
JFC International is recalling Fizzy Candy Punch Ramune because it may contain undeclared wheat allergen.
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
J F C International Inc started this food recall on 23 Nov 2016. The firm address in the FDA record is in Los Angeles, CA. FDA put the recall in Class II. FDA event 75788 has 2 product records. The first FDA enforcement report date is 21 Dec 2016. The record gives the status Terminated, with the termination date 11 Jan 2017.
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.
CA, CT, MA, NJ, and NY
Recalling firm
J F C International Inc, Los Angeles, CA.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
2 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0724-2017 | You-ka Fresh Ramune Net Wt. 3.87oz (110g), Item No. 23925, 20 packs/case | 391 packs | Class II | Terminated | 21 Dec 2016 |
| F-0725-2017 | You-ka Punch Ramune Net Wt. 3.87oz (110g), Item No. 23926, 20 packs/case | 500 packs | Class II | Terminated | 21 Dec 2016 |
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 II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2016
- 799
- Share of these events in Class II
- 43%
- Product records in this event
- 2Median of the firm: 1
- Events of the firm on the register
- 12
Other events of the firm
Official channels
- FDA enforcement report F-0724-2017The 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 75788. https://recallregister.com/fda/ii/75788/. 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:
CA, CT, MA, NJ, and NY
- What quantity of product is in FDA event 75788?
- The event has 2 product records. The first record gives this quantity:
391 packs
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2016 have the same class?
- 43% of the 799 food events that started in 2016 are in Class II.