RecallRadar
ModerateReported April 22, 2026 (10 weeks ago)

Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles

Recalled by Island Kinetics, Inc. d.b.a. CoValence Laboratories

Drug recall

Island Kinetics, Inc. d.b.a. CoValence Laboratories

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Island Kinetics, Inc. d.b.a. CoValence Laboratories has recalled Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 22, 2026 and was initiated on April 1, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, with approximately 28,163 bottles affected. The company behind the recall is Island Kinetics, Inc. d.b.a. CoValence Laboratories, based in Chandler, AZ. The FDA describes the product as: “Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873 9.”

Why was Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles recalled?

According to the FDA, the stated reason for the recall is: “Failed Stability Specifications.”

What should you do?

If you think you may have bought Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, compare it against the product description and identifying codes (Lot#: 4228D2, 4229D1, Exp.: 07/31/2026 Lot#: 5147D2, Exp.: 04/30/2027) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Island Kinetics, Inc. d.b.a. CoValence Laboratories or your local health authority.

About this recall

This recall was distributed in AZ. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
April 22, 2026
Recall started
April 1, 2026
Distributed in
AZ
What was recalled
Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873 9.
Why it was recalled (as stated by the FDA)
Failed Stability Specifications
How to identify the affected product
Lot#: 4228D2, 4229D1, Exp.: 07/31/2026 Lot#: 5147D2, Exp.: 04/30/2027
Amount recalled
28,163 bottles

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles recalled?+

According to the FDA: Failed Stability Specifications

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: D-0487-2026. Information last synced from the FDA on July 5, 2026.

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