HIGH

CURAD Alcohol Prep Pads Recalled Over Subpotent Isopropyl Alcohol

CURAD recalled 1,639,996 alcohol prep pads on July 7, 2025. The recall addresses subpotent isopropyl alcohol levels that fall below labeled concentration. Consumers should stop using these products immediately.

Quick Facts at a Glance

Recall Date
July 7, 2025
Hazard Level
HIGH
Brands
CURAD ALCOHOL PREP PADS, Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider for guidance. Notification method: Letter

Product Details

CURAD Alcohol Prep Pads, Medium, 2-Ply, NDC 53329-827-30. Sold in cartons containing 5 boxes, with 30 boxes per case. Manufactured for Medline Industries, LP, in India.

The Hazard

The recalled alcohol prep pads have isopropyl alcohol levels below the labeled concentration. This subpotency may compromise the effectiveness of the product.

Reported Incidents

No specific incidents, injuries, or adverse effects have been reported related to this recall. The product is classified as a Class II recall.

What to Do

Consumers should stop using the CURAD Alcohol Prep Pads immediately. Contact Medline Industries, LP for guidance on disposal and further assistance.

Contact Information

For more information, call 1-800-633-5463 or visit www.curad.com. Additional details are available at the FDA recall page.

Key Facts

  • Recall date: July 7, 2025
  • Quantity recalled: 1,639,996 pads
  • Manufactured in India
  • Subpotent isopropyl alcohol levels
  • Class II recall

Safety Assessment

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

Product Classification

Product Details

Model Numbers
61224050002
UPC Codes
53329-827
53329-827-60
53329-827-36
+6 more
Affected States
ALL
Report Date
September 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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