Last Updated Apr 4, 2018 11:00 AM EDT
WASHINGTON — A Las Vegas company was ordered to pull its herbal supplements off the market because some of its products tested positive for salmonella, part of alinked to the ingredient . The mandatory recall is the first of its kind for the U.S. Food and Drug Administration.
The FDA said Tuesday that it took the rare step of ordering the recall because Triangle Pharmanaturals refused to cooperate with U.S. regulators. Companies typically comply with government requests and voluntarily recall tainted products.
Calls and an email to the company were not immediately returned Tuesday morning.
"This action is based on the imminent health risk posed by the contamination of this product with, and the refusal of this company to voluntarily act to protect its customers and issue a recall," said FDA Commissioner Scott Gottlieb in a statement.
This week's action marks the first time the FDA has ever formally ordered a food recall. Congress gave the FDA that authority in 2011 after a series of high-profile food outbreaks involving peanut butter,and other grocery staples.
Various brands of kratom supplements have been linked to nearly 90 cases of salmonella across 35 states, according to federal figures. Salmonella is a bacterial infection that causes fever, cramps, diarrhea and nausea and can be life-threatening. Nearly 30 cases of the current outbreak have resulted in hospitalization, the Centers for Disease Control and Prevention reports.
Three other manufacturers have complied with a voluntary recall, CBS News' Anna Werner reports.
What is kratom?
Kratom is made from a plant native to Southeast Asia. Sold in various capsules and powders, kratom has gained popularity in the U.S. as an alternative treatment for pain,, drug dependence and even opioid withdrawal.
The FDA has been cracking down, stating that kratom has no approved medical use and, the class of addictive drugs behind the current nationwide epidemic of drug abuse.
Since kratom is considered a dietary supplement, not a drug, it has not been subject to the same federal requirements to prove its safety or whether it works.is also a risk.
"The issue is that they're not subject to pre-market safety testing, so unlike prescription drugs they've not been shown to be safe or effective," Chuck Jones, the Consumers Union program director, told CBS News.
"We continue to have serious concerns about the safety of any kratom-containing product and we are pursuing these concerns separately," Gottlieb said.
State and federal officials detected salmonella in a half-dozen samples of Triangle's products. But the company refused to allow FDA inspectors to access the company's records or discuss the contamination issue, according to an agency statement.
The FDA notified the company on Friday that it had 24 hours to halt distribution and begin its own recall of kratom-containing products, such as Raw Form Organics Maeng Da Kratom Emerald Green. The FDA said it ordered the recall on Monday after the company did not respond.
Consumers who have one or more of these products in their home should throw them away immediately. As an additional precaution, the FDA recommends kratom no longer stored in its original packaging should be discarded and the containers used to store it be thoroughly sanitized. After handling these products, people should wash their hands thoroughly, as well as work surfaces and utensils after contact.