"wu Yu" Kremezin Rapid-dissolving Tablets, 500 Mg

Kremezin Tablets Recall Summary Two batches of Kremezin 500mg tablets (batch numbers TT24Y05 and TT24Z13) are being recalled due to a discrepancy found in how residual solvent (ethanol) levels were tested during manufacturing. Although the recalled batches currently meet quality standards and no adverse events have been reported, the manufacturer is voluntarily recalling them as a precautionary measure to ensure medication safety.

Recalling firm

Xingchang Pharmaceutical Technology Co., Ltd.

Product

Batch: TT24Y05、TT24Z13，共2批藥品。. License: 衛部藥輸字第028080號

Reason

The manufacturer voluntarily reported that it had been notified by the original manufacturer that there was a deviation in the testing method for solvent (ethanol) residues in the manufacturing process of the drug in question. Although it has been confirmed that the drug from the batch in question meets specifications and no related adverse events have been reported, a precautionary recall has been initiated to ensure drug quality and patient safety.

Classification

Class II

Category

drug recall

Country

Taiwan

Agency

TFDA

Recall date

2026-06-10

Status

Ongoing

Official recall notice from TFDA

Recall details on Nibble Recalls: https://trynibble.app/recalls/9e235643-7dea-43d7-857c-a57e6ee8f588