HIGH

AUM Pharmaceuticals Recalls Alcohol Prep Pads Due to cGMP Deviations

AUM Pharmaceuticals recalled 50,000 cartons of Quick Touch Alcohol Prep Pads on July 21, 2025, due to cGMP deviations. The recall affects sterile pads containing 70% isopropyl alcohol. Consumers should stop using the product immediately and contact the manufacturer.

Quick Facts at a Glance

Recall Date
July 21, 2025
Hazard Level
HIGH
Brand
YANGZHOU YULOU PAPER PRODUCTS CO.
Category
Health & Personal Care
Sold At
Multiple Retailers
At-Risk Groups
GENERAL

Hazard Information

cGMP Deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact YANGZHOU YULOU PAPER PRODUCTS CO., LTD or your healthcare provider for guidance. Notification method: Letter

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Product Details

The recall involves Quick Touch Alcohol Prep Pads, Lot #: 20240610, and an expiration date of June 2029. The product comes in cartons containing 100 sterile pads each. A total of 500 cases were distributed.

The Hazard

The recall stems from deviations in current Good Manufacturing Practices (cGMP), which could compromise product safety and efficacy. Such deviations can lead to contamination or reduced potency of the alcohol prep pads.

Reported Incidents

No specific incidents or injuries have been reported related to this recall. However, the potential risks associated with cGMP deviations warrant immediate action.

What to Do

Consumers should stop using the Quick Touch Alcohol Prep Pads immediately. For further guidance, contact YANGZHOU YULOU PAPER PRODUCTS CO., LTD or consult a healthcare provider.

Contact Information

For assistance, reach out to YANGZHOU YULOU PAPER PRODUCTS CO., LTD. More information is available at the FDA's official recall notice.

Key Facts

  • Recall Date: July 21, 2025
  • Manufacturer: AUM Pharmaceuticals
  • Hazard: cGMP Deviations
  • Quantity Recalled: 500 cases
  • Contact for Guidance: YANGZHOU YULOU PAPER PRODUCTS CO., LTD

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Safety Assessment

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

Product Classification

Product Details

Model Numbers
Lot #: 20240610
Exp. Date 06/2029
Report Date
October 1, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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