Fresh Recalls

PureLife: recall status

Notice names this product. Keystone Industries’s PureLife is named in FDA Class II recall D-0605-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Defective container:may contain bottles with incomplete seals Identifying details: BNZ-001921, EXP 04/15/2029. Units affected: 450 units. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
PureLife
Company / brand
Keystone Industries
Lot / serial / date codes
BNZ-001921, EXP 04/15/2029
Distribution
Nationwide in the USA
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand
Keystone Industries

Recalls naming this model

FDA Class II · Drug · June 24, 2026

PureLife recall — Keystone Industries

Defective container:may contain bottles with incomplete seals

Company / brand: Keystone Industries

Affected product: PureLife

Official ID D-0605-2026 · Official record ↗

See all Keystone Industries recalls →

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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.