Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes for external use. The U.S. FDA listing cites lack of assurance of sterility as the reason for recall. Consumers and healthcare providers should stop using this product immediately and contact the manufacturer for guidance.
Lack of Assurance of Sterility.
Consumers and healthcare providers should stop using this product immediately. Contact Taizhou Kangping Medical Science And Technology Co., Ltd. or your healthcare provider for guidance. Notification method: Letter
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BZK antiseptic towelettes are used for external antiseptic purposes in clinical or professional settings. They come in cartons of 100 and are intended for professional use.
Lack of sterility assurance could lead to infection or contamination when used externally, especially in clinical environments.
This recall is not part of a broader industry pattern at this time.
High-risk for healthcare settings. Requires immediate cessation and switching to verified sterile products. Could disrupt infection-control protocols.
FDA recall page with enforcement report D-0589-2025; manufacturer contact on recall notice.
Refunds or replacements typically processed within 4-8 weeks depending on supplier.
Keep packaging, purchase receipts, and recall notices; record dates of communication with manufacturer.
Model numbers: 220583459, 230553459, 232743459, 110523, 031524, 052224, 247793459. Distribution: New York. Quantity: 3.85 million cartons. NDC: 71310-111-01. Sold for professional use. Manufactured by Taizhou Kangping Medical Science And Technology Co. Ltd., Taizhou, Jiangsu, China. Recall date: 2025-07-22. Status: Active.
No specific injuries or incidents are listed in the provided data.
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