Elevate Oral Care Recalls Povi-One
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Elevate Oral Care Recalls Povi-One
Elevate Oral Care · Class II — Moderate Risk

Product Description
Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LLC, 346 Pike Road, Suite 6, West Palm Beach, FL 33411, NDC 57511-0611-1.
Reason for Recall
sub potency
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
Nationwide
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class II FDA recall has been issued for a pharmaceutical product from Elevate Oral Care, initiated on June 4, 2026. sub potency. This recall covers 8132 6-packs & 2262 2-packs, distributed nationwide. While not the highest severity, consumers should exercise caution and stop using the product until the recall is resolved.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.