Warning
Keystone Industries Recalls PureLife
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
Source: FDA
WarningRecall #D-0605-2026Drug / Pharmaceutical
Keystone Industries Recalls PureLife
Keystone Industries · Class II — Moderate Risk
Product Description
PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for Pure Life, LLC, Manufactured for PureLife LLC., Carson, CA 90810. NDC 68987-001-30
Reason for Recall
Defective container:may contain bottles with incomplete seals
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 in the USA
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
Keystone Industries has recalled a pharmaceutical product that the FDA classified as Class II affecting 450 units. The recall was initiated on May 21, 2026. Defective container:may contain bottles with incomplete seals. It was distributed nationwide. Class II recalls involve products that might cause a temporary health problem or pose only a slight threat of a serious nature. Consumers should discontinue use and contact the firm.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.