CLASS I Food recall · Reported 27 Sep 2023 · FDA Enforcement Report

LA Original - The Original, Nut Diet Max, Nuez de la India recalled

Obc Group is recalling LA Original - The Original, Nut Diet Max, Nuez de la India. The recall was initiated on 5 Sep 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesExp. Date 2024
Quantity recalledUnknown

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-1543-2023
FDA event ID
92919
Recalling firm
Obc Group, Doral, FL
Classification
Class I
Status
Terminated
Recall initiated
5 Sep 2023
FDA classified
19 Sep 2023
Reported
27 Sep 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Other

Timeline

5 Sep 2023Recall initiated by company
19 Sep 2023Classified by FDA+14 days
27 Sep 2023Published 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

Product appears to be Yellow Oleander instead of Nuez de la India as labeled.

Product as listed by the FDA

LA ORIGINAL - THE ORIGINAL, NUT DIET MAX, Nuez de la India

Where it was distributed

Domestic distribution only.

Questions about this recall

Is LA Original - The Original, Nut Diet Max, Nuez de la India recalled?

Yes. Obc Group recalled LA Original - The Original, Nut Diet Max, Nuez de la India on 5 Sep 2023. The recall is Class I and its status is Terminated. Recall number F-1543-2023.

Why was it recalled?

Product appears to be Yellow Oleander instead of Nuez de la India as labeled.

Which lots are affected?

Exp. Date 2024

Where was it sold?

Domestic distribution only.

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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