PureLife recall (Keystone Industries)
DrugClass IIOngoing
Summary: Keystone Industries is recalling 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: Defective container:may contain bottles with incomplete seals.
What is being 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
Why
Defective container:may contain bottles with incomplete seals
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
Nationwide in the USA
How to tell if yours is affected
BNZ-001921, EXP 04/15/2029
What to do
Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.
Recall facts
| Recall number | D-0605-2026 |
| Category | Drug |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | May 21, 2026 |
| Reported | June 24, 2026 |
| Company | Keystone Industries |
| Company location | Gibbstown, NJ, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 450 units |
More recalls from Keystone Industries · all drug recalls · recalls from May 2026