Keystone Industries — FDA Compliance Timeline

FDA action counts

Enforcement history

On 2026-06-24, Argus HQ recorded a FDA recall for Keystone Industries, rated "high" severity in Argus HQ's classification: Keystone Industries — Class II recall: DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Man… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for Keystone Industries, rated "high" severity in Argus HQ's classification: Keystone Industries — Class II recall: PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavo… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for Keystone Industries, rated "high" severity in Argus HQ's classification: Keystone Industries — Class II recall: Quala Dental Products, Topical Anesthetic Gel, 20 % Benzocaine, Strawberry Flavo… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for Keystone Industries, rated "high" severity in Argus HQ's classification: Keystone Industries — Class II recall: Burkhart topical anesthetic gel, benzocaine 20 %, Strawberry Flavor, 1 oz (30 mL… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for Keystone Industries, rated "high" severity in Argus HQ's classification: Keystone Industries — Class II recall: Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for Keystone Industries, rated "high" severity in Argus HQ's classification: Keystone Industries — Class II recall: safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flav… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. On 2026-06-24, Argus HQ recorded a FDA recall for Keystone Industries, rated "high" severity in Argus HQ's classification: Keystone Industries — Class II recall: Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Conten… An FDA recall record reflects a firm removing or correcting a product already in distribution because it does not meet FDA requirements. In total, Keystone Industries has 7 FDA events on file with Argus HQ across the sources Argus HQ currently tracks (FDA Warning Letters, recalls, drug/biologic approvals, and Form 483 inspection observations).

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Keystone Industries has 7 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event.

Frequently asked questions

Does Argus HQ track new FDA actions for Keystone Industries automatically?

Yes. Argus HQ ingests FDA sources daily, including FDA warning letters, recalls, drug and biologic approvals, and Form 483 inspection observations. When a new FDA action linked to Keystone Industries is observed, this page's event count and history update automatically.

How many FDA actions does Argus HQ track for Keystone Industries?

7 total: 0 warning letters, 7 recalls, 0 approval records, and 0 Form 483 inspection citations.

What is the most recent FDA action on file for Keystone Industries?

June 24, 2026. Argus HQ ingests new FDA enforcement records daily.

Has Keystone Industries had product recalls?

Yes, 7 recalls on file. See the full history below for each one.

Related enforcement actions

• Keystone Industries — Class II recall: Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Conten… →
• Keystone Industries — Class II recall: safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flav… →
• Keystone Industries — Class II recall: Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30… →
• Keystone Industries — Class II recall: Burkhart topical anesthetic gel, benzocaine 20 %, Strawberry Flavor, 1 oz (30 mL… →
• Keystone Industries — Class II recall: Quala Dental Products, Topical Anesthetic Gel, 20 % Benzocaine, Strawberry Flavo… →
• Keystone Industries — Class II recall: PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavo… →
• Keystone Industries — Class II recall: DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Man… →

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