HIGHFDA DRUG

World Perfumes Inc. Recalled Iodo Blanco Iodides First Aid Antiseptic Over Leaking Containers (2025)

World Perfumes Inc. recalled 3,900 bottles of Iodo Blanco Iodides First Aid Antiseptic in Florida after broken or leaking containers were reported. The recall covers iodine 2% antiseptic distributed by Essential Products. Consumers should stop use immediately and contact World Perfumes or a healthcare provider for guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
February 13, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
February 13, 2025
Hazard Level
HIGH
Brands
World Perfumes, Essential Products
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, INFANTS

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
World Perfumes, Essential Products
Product type
First Aid Antiseptic (Iodine)
Model numbers
Lot 230619, Exp 06/30/2026
Sizes
1 fl. oz (30 ml) per bottle
Sold at
Unknown
Where affected
FL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    February 13, 2025

  2. Reported by FDA DRUG

    September 17, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Defective Container: broken or leaking bottles.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact World Perfumes Inc. or your healthcare provider for guidance. Notification method: Letter

About This Product

First aid antiseptic with iodine, used to clean wounds. Typically used in home or clinical settings.

Why This Is Dangerous

Defective containers can break or leak, risking exposure to antiseptic and potential irritation or chemical contact.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers face risk of skin or eye irritation from leaking antiseptic; no injuries reported yet.

Practical Guidance

How to identify if yours is affected

  1. Check bottle size 1 fl oz (30 ml)
  2. Check NDC 70242-109-01 and Lot 230619
  3. Look for packaging from Essential Products and World Perfumes Inc.

Where to find product info

FDA recall page and label information on bottle; recall letter.

What timeline to expect

Refund/replacement timelines not specified; anticipate several weeks to a couple of months

If the manufacturer is unresponsive

  • File a complaint with FDA/ CPSC if needed
  • Consult attorney if damages occur

How to prevent similar issues

  • Verify NDC and Lot before purchase
  • Avoid products with damaged packaging
  • Buy from reputable sources with recall notices

Documentation advice

Keep recall letter, take photos of packaging and lot numbers

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Product Details

Product: Iodo Blanco Iodides First Aid Antiseptic, Mercury Free, Iodine 2%, 1 fl. oz (30 ml) per bottle. Distributor: Essential Products. Brand: World Perfumes. NDC: 70242-109-01. Lot: 230619. Expiration: 06/30/2026. Quantity: 3,900 bottles. Distribution: Florida.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Distributed in Florida
  • 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

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTINFANTSCHILDRENELDERLYPETS
Injury Types
BURNELECTRICALLACERATIONPOISONINGELECTRICALELECTRICAL

Product Details

Model Numbers
Lot 230619
Exp 06/30/2026
Affected States
FL
Report Date
September 17, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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