The Food and Drug Administration on Tuesday ordered a mandatory recall of a Las Vegas company's powdered
kratom products, because salmonella was found in the herbal supplement.
Not exact matches
Food and Drug Administration (FDA) Commissioner Dr. Scott Gottlieb isn't mincing words about
kratom, the increasingly popular herbal substance that's been hawked as an alternative to painkillers and anti-depressants by companies promoting its ostensible curative properties (and supposedly innate safety as a «natural,» plant - based
product).
Under
kratom's current legal status, it can't be marketed for therapeutic reasons, and there are no FDA - approved uses for the herbal
product.
«We continue to have serious concerns about the safety of any
kratom - containing
product and we are pursuing these concerns separately.»
Advocates for
kratom tend to argue that the FDA is protecting big pharmaceutical interests — or at the very least isn't keeping an open mind — by cracking down on the
product.
The agency warned last fall that there's little evidence to support
kratom's use as a «natural» pain relief alternative, and in February, it issued a public health advisory saying that
kratom compounds — ostensibly meant to replace addictive opioid
products — are actually opioid
products themselves.
The FDA
kratom recall is aimed at a company called Triangle Pharmanaturals LLC after some
products from the company were found to contain salmonella, according to the agency.
Often used to help people with opioid addiction,
kratom (which can be bought online or in a vending machine) has caused at least 36 deaths because the
product is unregulated and being used without instruction.