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
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
- Brand
- Todrganic
- 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 2023 | Recall initiated by company | |
| 13 Sep 2023 | Classified by FDA | +19 days |
| 20 Sep 2023 | 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
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.
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