Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873
Summary
The FDA issued a Class II for Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Scrip by Island Kinetics, Inc. d.b.a. CoValence Laboratories. Reason: Failed Stability Specifications.
Details
Source
Drug Recall
External ID
D-0487-2026
Action Date
2026-04-22
Status
Ongoing
Category
drug
Product Description
Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873 9.
Lot/Code Info: Lot#: 4228D2, 4229D1, Exp.: 07/31/2026 Lot#: 5147D2, Exp.: 04/30/2027
Quantity Affected: 28,163 bottles
Reason for Recall
Failed Stability Specifications
Distribution
U.S. Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-01
Company
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 94 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
Island Kinetics, Inc. d.b.a. CoValence Laboratories has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Island Kinetics, Inc. d.b.a. CoValence Laboratories) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Island Kinetics, Inc. d.b.a. CoValence Laboratories have FDA actions?
Island Kinetics, Inc. d.b.a. CoValence Laboratories has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0487-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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