Bell Pharmaceuticals Recalls Clinere
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Bell Pharmaceuticals Recalls Clinere
Bell Pharmaceuticals, Inc · Class II — Moderate Risk

Product Description
Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%, 0.5 fl. oz. (15 mL); b) 1 bottle of Clinere Carbamide Peroxide (0,50 fl. oz. (15 mL), Dist. by: Quest Products LLC, Pleasant Prairie, WI 53158, NDC 68229-102-01.
Reason for Recall
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
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
U.S 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 Bell Pharmaceuticals, Inc, initiated on June 25, 2026. SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%). This recall covers 29, 474 units, distributed in U.S 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.