HIGH

Taizhou Kangping Medical Recalls Antiseptic Towelettes for Sterility Issues

Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes on July 22, 2025. The recall stems from a lack of assurance of sterility, posing a high risk to users. Consumers and healthcare providers must stop using these towelettes immediately.

Quick Facts at a Glance

Recall Date
July 22, 2025
Hazard Level
HIGH
Brand
Taizhou Kangping Medical Science And Technology Co.
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Lack of Assurance of Sterility.

What You Should Do

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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Product Details

The recall involves BZK Antiseptic Towelettes containing benzalkonium chloride 0.13%. The affected lot numbers are 220583459, 230553459, 232743459, 110523, 031524, 052224, and 247793459. These products were distributed in New York.

The Hazard

The recalled antiseptic towelettes lack assurance of sterility. This poses a significant health risk, especially in professional settings where sterility is critical.

What to Do

Stop using the affected towelettes immediately. Contact Taizhou Kangping Medical Science And Technology Co., Ltd. or your healthcare provider for further guidance.

Contact Information

For more information, reach out to Taizhou Kangping Medical at their official website or via the FDA's recall notice.

Key Facts

  • Recall date: July 22, 2025
  • Quantity recalled: 3.85 million cartons
  • Manufactured by Taizhou Kangping Medical
  • Distributed in New York

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
220583459
230553459
232743459
110523
031524
+2 more
Affected States
NY
Report Date
August 27, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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