FDAJanuary 28, 2020drug

Kushim Tablets (Gushim) 45-count packages, Label in foreign language

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Marketed Without an Approved NDA/ANDA. FDA analysis found product to contain cinobufagin, bufalin, and bufotenine

What to do

FDA enforcement status: Terminated

Brands named

b and a trading

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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