CLASS I ONGOING Food recall · Reported 9 Jul 2025 · FDA Enforcement Report
Bibimbap Bowl recalled by Jfe Franchising
Jfe Franchising is recalling Bibimbap Bowl 63912389259, distributed in 7 states. The recall was initiated on 20 May 2025 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0208-2025
- FDA event ID
- 96933
- Recalling firm
- Jfe Franchising, Houston, TX
- Brand
- Bibimbap Bowl
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 20 May 2025
- FDA classified
- 1 Jul 2025
- Reported
- 9 Jul 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Salmonella
- Product category
- Other
Timeline
| 20 May 2025 | Recall initiated by company | |
| 1 Jul 2025 | Classified by FDA | +42 days |
| 9 Jul 2025 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Cucumbers have the potential to be contaminated with Salmonella.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
Bibimbap Bowl 13 oz 63912389259
Where it was distributed
AL, IL, IN, KY, MI, TN, WI
Questions about this recall
Is Bibimbap Bowl 63912389259 recalled?
Yes. Jfe Franchising recalled Bibimbap Bowl 63912389259 on 20 May 2025. The recall is Class I and its status is Ongoing. Recall number H-0208-2025.
Why was it recalled?
Cucumbers have the potential to be contaminated with Salmonella.
Which lots are affected?
Sell by 5/20/2025
Where was it sold?
AL, IL, IN, KY, MI, TN, WI
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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