CLASS I Food recall · Reported 20 Sep 2023 · FDA Enforcement Report

Todrganic Natural Products, Nuez DE LA India recalled by Todorganic

Todorganic is recalling Todrganic Natural Products, Nuez DE LA India, Natural Products, 12 Seeds 12 Semillas. The recall was initiated on 25 Aug 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 168, EXP 10/24 *Firm informed that it will be recalling all lots of product currently in the market.
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-1513-2023
FDA event ID
92934
Recalling firm
Todorganic, Middleburg, FL
Classification
Class I
Status
Terminated
Recall initiated
25 Aug 2023
FDA classified
13 Sep 2023
Reported
20 Sep 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Product category
Other

Timeline

25 Aug 2023Recall initiated by company
13 Sep 2023Classified by FDA+19 days
20 Sep 2023Published 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

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

Product as listed by the FDA

TODRGANIC Natural Products, NUEZ DE LA INDIA, Natural Products, 12 Seeds 12 Semillas

Where it was distributed

Domestic distribution only.

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot 168, EXP 10/24 *Firm informed that it will be recalling all lots of product currently in the market.

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 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.

Other Other recalls

All 4,664