The company found an oxycodone pill when it was clearing a production line, the FDA says.
KVK-Tech, Inc. is voluntarily recalling a single lot of 10-milligram Betaxolol tablets"as a precautionary measure," after a single oxycodone hydrochloride tablet was found in one lot of the drug, according to the US Food and Drug Administration.KVK-Tech, Inc.
“The betaxolol package insert warns about slowing in the heart rate in elderly patients which is likely to be exacerbated by inadvertent opioid administration,” the FDA release warns. “Additionally, some patients prescribed low-dose betaxolol might have compromised heart and lung function that is also likely to be exacerbated by an opioid.”
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