Product Recalls

Recalls

On this page you’ll find recent recall alerts for food and feed products distributed or produced in Georgia. These alerts include the reason for the recall, a description of the issue, and a complete listing of affected products with identifying information. 

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G.A. Mart (H&Natural) (02/23/2024)

G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native to Mexico and Central America.

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Risk Statement: Ingestion of yellow oleander can cause neurologic, gastrointestinal and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia and more.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

H&NATURAL TejoRoot and H&NATURAL Brazil Seed were distributed Nationwide to via internet at https://www.handnatural.com, Amazon.com, and Walmart.com.

The recalled dietary supplements can be identified by the H&NATURAL logo and the following descriptions:

  • Tejo Root, Raiz de Tejocte, H&Natural, Healthy and Natural, Dietary Supplement, 10g pills, is packaged in a box or bottle, with UPC (196852946921)
  • Brazil Seed Pure Natural Semilla de Brasil, H& Natural, Healthy and Natural, 0.167g seeds, packaged in a box or bottle, with UPC (195893047529) (196852820641) (195893698721) (195893236893)(196852134618) (195893336975)

Recalled lots are labeled with the following expiration dates, 3/24 and 5/24.

Consumers with questions regarding this recall can contact G.A. Mart by phone at (928)389-4805 or ag@gamartgroup.com on Monday through Friday from 9 am to 5 pm, MST.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

  • Complete and submit the report Online
  • Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Link to Advisory (English Translation)

Link to Advisory (Spanish Translation)

 

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