The US FDA is addressing lax testing practices by healthcare product manufacturers following a review of regulatory alerts.
At least 28 companies have been reprimanded this year for failing to prove sufficient testing of ingredients used in over-the-counter drugs and consumer products for ethylene glycol (EG) and diethylene glycol (DEG), according to a Reuters analysis of agency import alerts and warning letters to manufacturers.
The manufacturers include US-based companies and exporters from India, South Korea, Switzerland, Canada and Egypt.
The FDA has flagged more manufacturers for failing to test raw materials susceptible to EG and DEG contamination in 2023 than in the previous five years combined, the Reuters analysis found.
The FDA told Reuters it has no indication products contaminated with DEG and EG have entered the US supply chain, and that the number of warning letters issued in a given period “is not a comprehensive marker of our oversight.”
Peter Lindsay, a lawyer at Paul Hastings in Washington, DC who specialises in FDA regulation and compliance, said to better spot contamination the agency was now requiring manufacturers to check individual containers of ingredients rather than just sampling raw materials.
“They’re upping the bar a little bit and trying to get industry to understand and recognize some of the risks in these areas,” he said.
Cough syrups made in India and Indonesia have been linked to the deaths of more than 300 children globally. The medicines were found to contain high levels of DEG and EG, leading to acute kidney injury and death.
The poisonings have sparked criminal probes, lawsuits and a surge in regulatory scrutiny worldwide. Reuters reported earlier this month that some Indian drugmakers involved could not prove they had purchased pharmaceutical-grade ingredients or tested their medicines for the toxins.
In the United States, more than 100 people, most of them children, died in the 1930s from DEG poisoning, prompting laws that greatly enhanced the FDA’s regulatory power over drugs.
Yet the agency did not establish explicit rules to test high-risk ingredients like propylene glycol (PG) and sorbitol solution for EG and DEG until May 2023.
Previous guidance from 2007 recommended certain tests be performed on glycerin, another common ingredient in over-the-counter drugs and consumer goods, to prevent the distribution of DEG-contaminated products. It now requires the same scrutiny of PG and other high-risk components for DEG and EG.
Import alerts
The FDA warning letters give manufacturers an opportunity to fix quality control problems or face penalties.
The letters sent to the 28 US and foreign manufacturers threaten to block either exports or imports of their products and new drug applications from those firms if they do not improve testing practices.
Half of them also received import alerts, which prohibit at-risk products from entering the country by allowing customs officials to detain them without examination.
Eleven of the manufacturers cited by the FDA this year marketed some of their at-risk products to children, including diarrhoea and pink eye medicines, toothpaste and sunscreen, according to the letters.
Florida-based Lex, a contract manufacturer of cough and cold medicines that can be used by children, was called out by the FDA on Aug. 17 for lax testing and repeated quality-control violations going back to 2004.
Lex co-owner Charlene Paz said the company has addressed the shortcomings identified by the FDA and is conducting all required tests for impurities whenever they get ingredients susceptible to EG and DEG contamination.
Fourteen foreign manufacturers that sold products susceptible to DEG and EG poisoning were placed on import alert lists for failure to prove sufficient quality control. They include South Korea’s LCC, which makes Oriox and other mouthwashes, and India-based toothpaste manufacturers Suhan Aerosol and Orchid Lifesciences.
