CLASS III Food recall · Reported 19 Mar 2025 · FDA Enforcement Report
Mi More snacks, Coco Bandera, 8 per container recalled
San Miguel Nuts is recalling Mi More snacks, Coco Bandera, 8 per container, distributed in New Jersey. The recall was initiated on 4 Dec 2024 and the FDA has classified it as Class III.
Recall details
- Recall number
- F-0629-2025
- FDA event ID
- 96254
- Recalling firm
- San Miguel Nuts, Passaic, NJ
- Brand
- Mi More
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 4 Dec 2024
- FDA classified
- 13 Mar 2025
- Reported
- 19 Mar 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Visit
- Reason category
- Undeclared Allergens
- Product category
- Other
Timeline
| 4 Dec 2024 | Recall initiated by company | |
| 13 Mar 2025 | Classified by FDA | +99 days |
| 19 Mar 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared color on label
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Mi More snacks, Coco Bandera, 3 oz. Plastic container, 8 per container, 20 per case box
Where it was distributed
The recalled product was distributed to the following states: NJ
Questions about this recall
Is Mi More snacks, Coco Bandera, 8 per container recalled?
Yes. San Miguel Nuts recalled Mi More snacks, Coco Bandera, 8 per container on 4 Dec 2024. The recall is Class III and its status is Terminated. Recall number F-0629-2025.
Why was it recalled?
Undeclared color on label
Where was it sold?
The recalled product was distributed to the following states: NJ
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
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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