The U.S. Food and Drug Administration (FDA) announced the recall of a common medication used to treat heartburn and stomach problems because of possible contamination.
Contaminated products could potentially cause intestinal distress, including abdominal pain or diarrhea, although individuals with compromised immune systems have a chance of developing a widespread infection if they ingest or are exposed to the products, the FDA warned.
But so far, according to the FDA, Plastikon hasn’t received any customer complaints related to microbial concerns or reports of adverse incidents in connection to the recalled products.
“Plastikon Healthcare places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process,” the FDA said.
Plastikon recommended that customers return all recalled products to the place of purchase. Patients are advised to contact their doctor or health care provider if they have any problems in connection to the contaminated products, it said.
The FDA has placed the recalled product labels and lot numbers on its website.
“The product is packaged for institutional use and is sold to clinics and hospitals nationwide in single-use cups with a foil lid,” the agency said. “The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 5/1/2020 and 6/28/2021, who shipped to hospitals, nursing homes, and clinics nationwide. The products are private labeled for Major Pharmaceuticals.”
The statement indicated the recall was initiated due to nitrosamines, which can lead to increased cancer risk, and the firm believes the “benefit/risk profile of the products remains positive based on currently available data.”
“Although long-term ingestion of N-nitroso-quinapril may be associated with a potential increased cancer risk in humans, there is no immediate risk to patients taking this medication,” it said.