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
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0605-2026
- Classification
- Class II
- Recalled
- May 21, 2026
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