Jon Styf  |  November 1, 2023

Category: Legal News
Close up of a woman's hand holding white capsules, representing the Botanical-Be supplements recall.
(Photo Credit: Farknot Architect/Shutterstock)

Botanical-Be recall overview: 

  • Who: Botanical-Be recalled its Kuka Flex Forte, Artri King and Reumo Flex capsules. 
  • Why: The capsules all included diclofenac, an unapproved and unlisted Non-Steroidal Anti-Inflammatory drug (NSAID).
  • Where: The Botanical-Be recall applies across the United States.

Botanical-Be announced a recall of its Kuka Flex Forte, Artri King and Reumo Flex capsules because the products contain diclofenac, a Non-Steroidal Anti-Inflammatory drug (NSAID), making the capsules unapproved drugs.

An analysis from the U.S. Food and Drug Administration (FDA) found the presence of diclofenac, which is unapproved because the FDA has not established its safety and efficacy.

The recall applies to Artri King in 100-capsule bottles, Kuka Flex in 30-capsule bottles and Reumo flex in 30-capsule bottles. The products are dietary supplements for relief of pain and inflammation, according to the recall notice.

The lot numbers and expirations are 

  • Artri King: lot 35421 with an expiration date of Dec. 19, 2025
  • Kuka Flex Forte: all lots with an expiration date of Dec. 12, 2024, and UPC code 0736640810265
  • Reumo Flex: all lots with an expiration date of Oct. 20, 2024

Consuming diclofenac can lead to serious health risks, supplement recall states

Botanical-Be says it has not received any reports of illness related to the recall. The company is not facing legal action over the recall, but Top Class Actions follows recalls closely as they sometimes lead to class action lawsuits.

Consuming diclofenac without knowledge could lead to serious health risks, including cardiovascular, gastrointestinal and renal problems and anaphylaxis, according to the supplements recall notice.

Consumers can contact Botanical-Be at (915) 412-6237‬ or by email at botanical.be@gmail.com from 8 a.m. to 5 p.m. MT.

In other supplement recalls, the FDA announced an urgent recall in March of Dr. Rima Recommends Nano Silver 10 ppm dietary supplement as the product makes “unsubstantiated health claims that the product will prevent, treat or cure COVID-19.” 

Are you affected by the Botanical-Be recall? Let us know in the comments. 


Don’t Miss Out!

Check out our list of Class Action Lawsuits and Class Action Settlements you may qualify to join!


Read About More Class Action Lawsuits & Class Action Settlements:

We tell you about cash you can claim EVERY WEEK! Sign up for our free newsletter.

2 thoughts onBotanical-Be issues recall for supplements due to diclofenac presence

  1. LILLIE Lillie says:

    Add me

  2. Everett Scott says:

    Add me please

Leave a Reply

Your email address will not be published. By submitting your comment and contact information, you agree to receive marketing emails from Top Class Actions regarding this and/or similar lawsuits or settlements, and/or to be contacted by an attorney or law firm to discuss the details of your potential case at no charge to you if you qualify. Required fields are marked *

Please note: Top Class Actions is not a settlement administrator or law firm. Top Class Actions is a legal news source that reports on class action lawsuits, class action settlements, drug injury lawsuits and product liability lawsuits. Top Class Actions does not process claims and we cannot advise you on the status of any class action settlement claim. You must contact the settlement administrator or your attorney for any updates regarding your claim status, claim form or questions about when payments are expected to be mailed out.