DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz
Defective container:may contain bottles with incomplete seals
- Agency
- FDA Drug
- Recall date
- May 21, 2026
- Status
- Ongoing
- Company
- Keystone Industries
1. What product was recalled?
Burkhart topical anesthetic gel, benzocaine 20 %, Strawberry Flavor, 1 oz (30 mL), Manufactured for Burkhart Dental Supply, Tacoma, Washington, 98409
Burkhart topical anesthetic gel, benzocaine 20 %, Strawberry Flavor, 1 oz (30 mL), Manufactured for Burkhart Dental Supply, Tacoma, Washington, 98409. NDC: 43498-310-30
Quantity: 150 units
Code or lot text: BNZ-001917, Exp 04/15/2029
- LOT
- BNZ-001917
- LOT
- Exp 04/15/2029
- NDC
- 43498-310
- NDC
- 43498-310-30
- RECALL-NUMBER
- D-0603-2026
DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz
DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Manufactured for and Distributed by Dental Health Products, Inc, 2614 North Sugar Bush Road, New Franken, WI 54229. NDC 69634-020-30
Quantity: 150 units
Code or lot text: BNZ-001921, EXP 04/15/2029
- LOT
- BNZ-001921
- LOT
- EXP 04/15/2029
- NDC
- 69634-020
- NDC
- 69634-020-30
- RECALL-NUMBER
- D-0602-2026
Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30 g), Distributed by Dental City, 3205 Yeager Dr
Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30 g), Distributed by Dental City, 3205 Yeager Dr., Green Bay, WI 54311. NDC 69483-001-30
Quantity: 450 units
Code or lot text: BNZ-001921, Exp 04/15/2029
- LOT
- BNZ-001921
- LOT
- Exp 04/15/2029
- NDC
- 69483-001
- NDC
- 69483-001-30
- RECALL-NUMBER
- D-0604-2026
Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Contents: 1 oz (3o g), Manufactured for: Pearson Dental Supply Inc
Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Contents: 1 oz (3o g), Manufactured for: Pearson Dental Supply Inc., Sylmar, CA 91342 USA, NDC 43305-0009-3.
Quantity: 900 units
Code or lot text: BNZ-001917, Exp 04/01/2029
- LOT
- BNZ-001917
- LOT
- Exp 04/01/2029
- NDC
- 43305-0009
- NDC
- 43305-0009-3
- RECALL-NUMBER
- D-0600-2026
PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for Pure Life, LLC, Manufactured for PureLife LLC
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
Code or lot text: BNZ-001921, EXP 04/15/2029
- LOT
- BNZ-001921
- LOT
- EXP 04/15/2029
- NDC
- 68987-001
- NDC
- 68987-001-30
- RECALL-NUMBER
- D-0605-2026
Quala Dental Products, Topical Anesthetic Gel, 20 % Benzocaine, Strawberry Flavor Net Contents: 1 oz (30 g), Quala Dental Products, Made in USA for NDC Inc
Quala Dental Products, Topical Anesthetic Gel, 20 % Benzocaine, Strawberry Flavor Net Contents: 1 oz (30 g), Quala Dental Products, Made in USA for NDC Inc., 407 Sanford Road, Le Vergne, TN 37086, NDC 43128-034-30.
Quantity: 150 units
Code or lot text: BNZ-001921, EXP 04/15/2029
- LOT
- BNZ-001921
- LOT
- EXP 04/15/2029
- NDC
- 43128-034
- NDC
- 43128-034-30
- RECALL-NUMBER
- D-0601-2026
safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flavor, 1 oz
safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flavor, 1 oz. (29.6mL), Distributed by: Safco Dental Supply Co., Buffalo Grove, IL 60099, Made in USA, NDC 67239-0223-1.
Quantity: 150 units
Code or lot text: BNZ-001921, Exp 04/15/2029
- LOT
- BNZ-001921
- LOT
- Exp 04/15/2029
- NDC
- 67239-0223
- NDC
- 67239-0223-1
- RECALL-NUMBER
- D-0606-2026
2. Is my exact product affected?
Compare every printed identifier. A matching value can indicate that your product is included.
3. What is the hazard?
Defective container:may contain bottles with incomplete seals
4. What should I do now?
Follow the FDA recall notice and contact the recalling company for current instructions.
5. Where was it sold or distributed?
Nationwide
6. Were injuries or illnesses reported?
No separate injury or illness statement was present in the normalized record. Check the official source for the latest report.
7. What remedy is available?
Follow the FDA recall notice and contact the recalling company for current instructions.
8. Is the recall active or closed?
The source status is Ongoing. Recall Index urgency is elevated, which is a separate deterministic site label.
9. When was the information checked?
Last checked .
- updated
- created
10. Where is the official source?
Open the official FDA Drug source
Recall Index normalizes public source data for easier checking. Source agencies remain authoritative. Confirm identifiers and instructions at the official source.