FDA recalls nearly 370,000 bottles of popular antidepressant over carcinogen contamination

Nearly 370,000 bottles of popular antidepressant Duloxetine are recalled due to high levels of cancer-causing compounds. The US FDA issued a Class II recall for specific batches of 30 mg and 60 mg capsules. While the contaminant is suspected of causing cancer, experts note exposure risks are linked to long-term, high-level intake. Patients should consult their doctor before discontinuing medication.

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