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FDA · Drugs ·

PureLife recall

Keystone Industries recalled PureLife on June 24, 2026 because of defective container:may contain bottles with incomplete seals. It was sold nationwide.

Why it was recalled

Defective container:may contain bottles with incomplete seals

What's recalled

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

Quantity: 450 units

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Keystone Industries, Gibbstown, NJ
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
Nationwide in the USA
Status
Ongoing
Recall number
D-0605-2026
Source
U.S. Food and Drug Administration

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