HIGHFDA DRUG

READYPREP PVP Iodine 10% Topical Antiseptic Recalled for Subpotent Drug (Medline)

FDA recalls READYPREP PVP, povodone-iodine 10% topical antiseptic. Medline Industries issued the nationwide recall. Subpotent drug is the reason. Consumers should stop using the product immediately.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
August 19, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
August 19, 2025
Hazard Level
HIGH
Brands
POVIDONE-IODINE, Medline Industries
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

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
POVIDONE-IODINE, Medline Industries
Product type
Topical antiseptic solution
Model numbers
Lot # 24EJA180, Exp 06/01/2027
UPC codes
53329-939, 53329-939-04, 53329-939-06, 53329-939-08, 53329-939-23, 53329-939-25, 53329-939-69, 53329-939-13
Sizes
1 Gallon (3.78 L) per bottle
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    August 19, 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

Subpotent drug

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Medline Industries, LP or your healthcare provider for guidance. Notification method: Letter

About This Product

READYPREP PVP is a povidone-iodine 10% topical antiseptic intended for cleaning wounds and skin disinfecting in medical settings and at home.

Why This Is Dangerous

Subpotent drug may not deliver expected antiseptic effect, potentially increasing infection risk in use.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

If used in clinical or home care, reduced efficacy could necessitate additional treatment and monitoring.

Practical Guidance

How to identify if yours is affected

  1. Check NDC 53329-939-25 on the label.
  2. Verify Lot number 24EJA180.
  3. Confirm Expiration Date 06/01/2027.
  4. Ensure bottle is 1 gallon (3.78 L).

Where to find product info

NDC and lot info located on label; recall page provides details.

What timeline to expect

Remedy details communicated via recall letter; replacement or refund timelines depend on Medline notification.

If the manufacturer is unresponsive

  • File a complaint with FDA if manufacturer is unresponsive.
  • Consider contacting your clinician for interim antiseptic alternatives.

How to prevent similar issues

  • Buy sterile antiseptics from reputable brands.
  • Verify lot numbers before use.
  • Store per label instructions to maintain potency.

Documentation advice

Keep packaging, recall letter, and any correspondence with Medline for records.

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

Product: READYPREP PVP, povidone-iodine 10% solution. Package: 1 gallon (3.78 L) bottles. Manufacturer: Medline Industries, LP. Location: United States. NDC: 53329-939-25. Lot: 24EJA180. Expiration: 06/01/2027. Quantity: 2,680 bottles. Distribution: Nationwide in the USA.

Reported Incidents

No injuries or incidents have been reported in the recall notice.

Key Facts

  • High hazard level

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

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

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

Product Details

Model Numbers
Lot # 24EJA180
Exp 06/01/2027
UPC Codes
53329-939
53329-939-04
53329-939-06
+5 more
Affected States
ALL
Report Date
October 1, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

Related Recalls