TODRGANIC Natural Products, NUEZ DE LA INDIA, Natural Products, 12 Seeds 12 Semillas
Summary
The FDA issued a Class I for TODRGANIC Natural Products, NUEZ DE LA INDIA, Natural Products, 12 Seeds 12 Semi by Todorganic Inc.. Reason: Product appears to be Yellow Oleander instead of Nuez de la India as labeled..
Details
Source
Food Recall
External ID
F-1513-2023
Action Date
2023-09-20
Status
Terminated
Category
food
Product Description
TODRGANIC Natural Products, NUEZ DE LA INDIA, Natural Products, 12 Seeds 12 Semillas
Lot/Code Info: Lot 168, EXP 10/24 *Firm informed that it will be recalling all lots of product currently in the market.
Quantity Affected: Unknown
Reason for Recall
Product appears to be Yellow Oleander instead of Nuez de la India as labeled.
Distribution
Domestic distribution only.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-25
Company
Middleburg, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Todorganic Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Todorganic Inc. have FDA actions?
This is the only FDA action we have on record for Todorganic Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1513-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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