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Medium risk Drugs & MedicationsClass II

PureLife Benzocaine Topical Anesthetic Recall

PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for Pure Life, LLC, Manufactured for PureLife

Updated May 21, 2026

PureLife Topical Anesthetic Gel (Benzocaine 20%, 1 oz, Strawberry Flavor) is being recalled because some bottles may have incomplete seals, which could allow contamination or leakage. If you have this product, do not use it.

Is the Keystone Industries recalled? Yes. This product was recalled by FDA on May 21, 2026. Details below.

What is recalled

PureLife Topical Anesthetic Gel, Benzocaine 20%, 1 oz (30 mL), Strawberry Flavor. Manufacturer: Pure Life, LLC, Carson, CA 90810. NDC 68987-001-30.

Am I affected

You are affected if you own a 1 oz (30 mL) bottle of PureLife Topical Anesthetic Gel with Benzocaine 20% in Strawberry Flavor and NDC 68987-001-30 on the label.

What to do right now

Stop using this product immediately. Dispose of it safely or contact the seller or manufacturer for instructions on return or replacement.

The hazard

Defective container:may contain bottles with incomplete seals

Brands affected

Keystone Industries
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0605-2026
Classification
Class II
Recalled
May 21, 2026
Read the official notice

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