Information
Island Kinetics Recalls Skin Rehab
This is a Class III recall. This product is unlikely to cause adverse health reactions but violates FDA regulations.
Source: FDA
InfoRecall #D-0481-2026Drug / Pharmaceutical
Island Kinetics Recalls Skin Rehab
Island Kinetics, Inc. d.b.a. CoValence Laboratories · Class III — Regulatory
Product Description
Skin Rehab, Calming Skin Gel, Hydrocortisone Balm, hydrocortisone 1%, .53oz net wt. (15.3g) per bottle, Distributed By: A.C.E. Inc., DFW Intl. Airport, Texas 75261, www.RHONDAALLISON.COM. NDC 66915-531-04
Reason for Recall
Subpotent Drug
FDA Classification
Class III — Regulatory
A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Distribution
U.S. Nationwide
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A regulatory compliance recall has been issued for a pharmaceutical product from Island Kinetics, Inc. d.b.a. CoValence Laboratories. The FDA classified this as Class III on March 18, 2026 affecting 2895 bottles. Subpotent Drug. It was distributed in U.S. Nationwide. While this classification indicates a low probability of adverse health effects, consumers should be aware of the recall and follow any instructions from the manufacturer.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.