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 2024Recall initiated by company
13 Mar 2025Classified by FDA+99 days
19 Mar 2025Published 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

New Jersey

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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