Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 99076

7 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 21, 2026
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Keystone Industries

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

7 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 7

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.

D-0600-2026
Recall number
D-0600-2026
Initiated
May 21, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Keystone Industries
Quantity
900 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container:may contain bottles with incomplete seals

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective container:may contain bottles with incomplete seals

Code information

BNZ-001917, Exp 04/01/2029

Distribution pattern

Nationwide in the USA

drug · product 2 of 7

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.

D-0601-2026
Recall number
D-0601-2026
Initiated
May 21, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Keystone Industries
Quantity
150 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container:may contain bottles with incomplete seals

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective container:may contain bottles with incomplete seals

Code information

BNZ-001921, EXP 04/15/2029

Distribution pattern

Nationwide in the USA

drug · product 3 of 7

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

D-0602-2026
Recall number
D-0602-2026
Initiated
May 21, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Keystone Industries
Quantity
150 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container:may contain bottles with incomplete seals

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective container:may contain bottles with incomplete seals

Code information

BNZ-001921, EXP 04/15/2029

Distribution pattern

Nationwide in the USA

drug · product 4 of 7

Burkhart topical anesthetic gel, benzocaine 20 %, Strawberry Flavor, 1 oz (30 mL), Manufactured for Burkhart Dental Supply, Tacoma, Washington, 98409. NDC: 43498-310-30

D-0603-2026
Recall number
D-0603-2026
Initiated
May 21, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Keystone Industries
Quantity
150 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container:may contain bottles with incomplete seals

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective container:may contain bottles with incomplete seals

Code information

BNZ-001917, Exp 04/15/2029

Distribution pattern

Nationwide in the USA

drug · product 5 of 7

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

D-0604-2026
Recall number
D-0604-2026
Initiated
May 21, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Keystone Industries
Quantity
450 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container:may contain bottles with incomplete seals

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective container:may contain bottles with incomplete seals

Code information

BNZ-001921, Exp 04/15/2029

Distribution pattern

Nationwide in the USA

drug · product 6 of 7

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

D-0605-2026
Recall number
D-0605-2026
Initiated
May 21, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Keystone Industries
Quantity
450 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container:may contain bottles with incomplete seals

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective container:may contain bottles with incomplete seals

Code information

BNZ-001921, EXP 04/15/2029

Distribution pattern

Nationwide in the USA

drug · product 7 of 7

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.

D-0606-2026
Recall number
D-0606-2026
Initiated
May 21, 2026
Classification
Class II
Status
Ongoing
Recalling firm
Keystone Industries
Quantity
150 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Defective container:may contain bottles with incomplete seals

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Defective container:may contain bottles with incomplete seals

Code information

BNZ-001921, Exp 04/15/2029

Distribution pattern

Nationwide in the USA