H&NATURAL TEJOCOTE ROOT 90 PIECES, 3 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.
Summary
The FDA issued a Class I for H&NATURAL TEJOCOTE ROOT 90 PIECES, 3 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJO by HandNatural. Reason: Product recalled due to the presence of yellow oleander and its components in the product..
Details
Source
Food Recall
External ID
F-1161-2024
Action Date
2024-04-24
Status
Ongoing
Category
food
Product Description
H&NATURAL TEJOCOTE ROOT 90 PIECES, 3 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.
Lot/Code Info: No Lot code on label. Expiration date listed as 05/24 and 03/24.
Quantity Affected: Unknown at this time.
Reason for Recall
Product recalled due to the presence of yellow oleander and its components in the product.
Distribution
Firm is 100% internet sales. Distribution is unknown at this time.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-09
Company
San Luis, AZ
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 52 food recalls issued in the same week, part of 204 food-related FDA actions this month.
HandNatural has 15 FDA actions in our database, including 15 recalls.
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 (HandNatural) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HandNatural have FDA actions?
HandNatural has 15 FDA actions in our database, including 15 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1161-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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