CLASS II ONGOING Food recall · Reported 7 May 2025 · FDA Enforcement Report
Chile Verde Egg Bites recalled by Valley Fine Foods Co
Valley Fine Foods Co is recalling Chile Verde Egg Bites, distributed in Texas. The recall was initiated on 3 Apr 2025 and the FDA has classified it as Class II.
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
- F-0746-2025
- FDA event ID
- 96733
- Recalling firm
- Valley Fine Foods Co, Benicia, CA
- Brand
- Chile Verde
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 3 Apr 2025
- FDA classified
- 30 Apr 2025
- Reported
- 7 May 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Foreign Material
- Product category
- Eggs
Timeline
| 3 Apr 2025 | Recall initiated by company | |
| 30 Apr 2025 | Classified by FDA | +27 days |
| 7 May 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential contamination with foreign materials.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
CHILE VERDE EGG BITES; NET WT. 4.6 OZ (130 g); 2 egg bites/package
Where it was distributed
TX
Questions about this recall
Why was it recalled?
Potential contamination with foreign materials.
Which lots are affected?
UPC code: 0-41220-30655-8; Lot: 05/17/25 [time stamp] L2
Where was it sold?
TX
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 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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