HIGHFDA DRUG

AUM Pharmaceuticals Isopropyl Alcohol Prep Pads Recall: 500 Cases Active, High Hazard

A high-hazard recall is active for Quick Touch Alcohol Prep Pads. 500 cases are affected. The recall covers products from YANGZHOU YULOU PAPER PRODUCTS CO. and AUM Pharmaceuticals. Consumers should stop using immediately and consult healthcare providers for guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
July 21, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
AUM Pharmaceuticals, YANGZHOU YULOU PAPER PRODUCTS CO.
Product type
Alcohol Prep Pads
Model numbers
Lot #: 20240610, Exp. Date 06/2029
Colors
Unknown
Sizes
Unknown
Sold at
Multiple Retailers

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    July 21, 2025

  2. Reported by FDA DRUG

    October 1, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

Alcohol prep pads are sterile, used to prep skin before injections or medical procedures. They are widely used in clinical and home settings.

Why This Is Dangerous

cGMP deviations may compromise product sterility and consistency, potentially increasing infection risk if contaminated.

Industry Context

This recall is not clearly listed as part of a broader pattern in the provided data.

Real-World Impact

Consumers should stop using immediately. The recall is active and involves 500 cases.

Practical Guidance

How to identify if yours is affected

  1. Check carton label for Quick Touch Alcohol Prep Pads Isopropyl Alcohol 70% 100 sterile pads per carton

Where to find product info

FDA enforcement report link and recall notice (D-0659-2025)

What timeline to expect

Refunds or replacements, if offered, will follow standard FDA recall timelines, often several weeks to a few months

If the manufacturer is unresponsive

  • Document all communications
  • Escalate to FDA recall supervisor or consumer protection agency

How to prevent similar issues

  • Verify sterility and cGMP compliance for medical supplies
  • Purchase from reputable suppliers with clear lot and expiry information
  • Retain packaging and lot numbers for recalls

Documentation advice

Keep photos of packaging, lot, expiry, and all correspondence

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Product Details

Product: Quick Touch Alcohol Prep Pads (Isopropyl Alcohol 70%). 100 sterile pads per carton. Manufacturer: AUM Pharmaceuticals, 320 Oser Ave., Hauppauge, NY 11788. Distributor: YANGZHOU YULOU PAPER PRODUCTS CO., LTD. Quantity: 500 cases. Recall status: Active. Recall date: 2025-07-21. Expiry date: 06/2029. Lot number: 20240610.

Reported Incidents

No injuries or incidents have been reported in the provided information.

Key Facts

  • High hazard level
  • Class II recall

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
GENERALPREGNANTPETS
Injury Types
OTHER

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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