Keystone Industries 2026-06-24 Health serious FDA
Health · FDA · Recall #FDA-D-0605-2026
PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor,… Recall
Issued June 24, 2026 · Keystone Industries
In June 2026, Keystone Industries recalled the PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor,…, a serious health recall reported by the FDA.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
Defective container:may contain bottles with incomplete seals
What you should do
- 1 Stop using PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Keystone Industries to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Keystone Industries
- Category
- Health
- Recall date
- June 24, 2026
- Units affected
- Not reported
- Sold at
- Nationwide in the USA
- Recall number
- FDA-D-0605-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Keystone Industries has 10 recalls in our database.
- We're tracking 3,673 Health recalls in our database.
- This is the 453rd Health recall we've logged in 2026.