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Class IIOngoing

Iodo Blanco Iodides recall

FDA recall D-0622-2025 · initiated Feb 13, 2025

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Sep 17, 2025How we research

World Perfumes Inc. recalled Iodo Blanco Iodides in Feb 2025 — an FDA Class II recall (D-0622-2025) because Defective Container: broken or leaking bottles.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

Defective Container: broken or leaking bottles.

Labelling, packaging or a product mix-up

The wrong information — or the wrong medicine — ended up in the pack. A mix-up is a manufacturing failure that can still be dangerous to swallow.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot 230619, Exp 06/30/2026

Quantity recalled: 3,900 bottles

Details

Product
Iodo Blanco Iodides, First Aid Antiseptic, Mercury Free, Iodine 2%, First Aid Antiseptic, Contains 1 fl. oz (30 ml) per bottle, Distributed by: Essential Products, www.essentialproductsusa.com, NDC: 70242-109-01
Recalling company
World Perfumes Inc.
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
FL
Initiated
Feb 13, 2025
FDA report date
Sep 17, 2025
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Iodo Blanco Iodides recalled?
World Perfumes Inc. recalled Iodo Blanco Iodides in Feb 2025 — an FDA Class II recall (D-0622-2025) because Defective Container: broken or leaking bottles. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Iodo Blanco Iodides recalled?
Per the FDA enforcement record, the reason for recall D-0622-2025 was: Defective Container: broken or leaking bottles.
Is a recalled Iodo Blanco Iodides dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Iodo Blanco Iodides are affected?
Distributed: FL. The recall covers these lots — Lot 230619, Exp 06/30/2026. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0622-2025.

Source: openFDA Drug Enforcement record D-0622-2025

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