FDA action counts
| Total FDA actions | 8 |
|---|---|
| Warning letters | 0 |
| Recalls | 8 |
| Approval records | 0 |
| Form 483 inspection citations | 0 |
| Most recent action | July 8, 2026 |
Enforcement history
On 2026-07-08, Argus HQ recorded an FDA recall for Blaine Labs Inc, rated "high" severity in Argus HQ's classification: Blaine Labs Inc — Class II recall: TERPENICOL Antifungal Cream (Undecylenic Acid 13%), 1.0 oz (28 g) bottles, Manuf…. On 2026-07-08, Argus HQ recorded an FDA recall for Blaine Labs Inc, rated "high" severity in Argus HQ's classification: Blaine Labs Inc — Class II recall: Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) pac…. On 2026-07-08, Argus HQ recorded an FDA recall for Blaine Labs Inc, rated "high" severity in Argus HQ's classification: Blaine Labs Inc — Class II recall: TRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl…. On 2026-07-08, Argus HQ recorded an FDA recall for Blaine Labs Inc, rated "high" severity in Argus HQ's classification: Blaine Labs Inc — Class II recall: TERPENICOL Antifungal Solution, (Undecylenic (10-Undecenoic) acid 25%), 1.0 Fl O…. On 2026-07-08, Argus HQ recorded an FDA recall for Blaine Labs Inc, rated "critical" severity in Argus HQ's classification: Blaine Labs Inc — Class I recall: Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37…. On 2026-07-08, Argus HQ recorded an FDA recall for Blaine Labs Inc, rated "high" severity in Argus HQ's classification: Blaine Labs Inc — Class II recall: TRIPENICOL S Antifungal Solution (Undecylenic Acid 25%), 1.25 FL OZ (37.5 mL) bo…. On 2026-07-08, Argus HQ recorded an FDA recall for Blaine Labs Inc, rated "high" severity in Argus HQ's classification: Blaine Labs Inc — Class II recall: Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x…. On 2026-07-08, Argus HQ recorded an FDA recall for Blaine Labs Inc, rated "high" severity in Argus HQ's classification: Blaine Labs Inc — Class II recall: vite20 Antifungal Cream, (10% Undecylenic Acid), 0.54 OZ (15 g) bottle, Manufact….
Risk pattern analysis
Argus HQ analysis — not an FDA finding
This section is Argus HQ analysis, not an FDA finding. Blaine Labs Inc has 8 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. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
Frequently asked questions
- What is the most recent FDA action on file for Blaine Labs Inc?
- July 8, 2026. Argus HQ ingests new FDA enforcement records daily.
- Has Blaine Labs Inc had product recalls?
- Yes, 8 recalls on file. See the full history below for each one.
- Is this FDA enforcement data for Blaine Labs Inc official?
- Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.
- How many FDA actions has Blaine Labs Inc had?
- Argus HQ has recorded 8 FDA events for Blaine Labs Inc: 0 warning letters, 8 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.
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Related enforcement actions
- Blaine Labs Inc — Class II recall: vite20 Antifungal Cream, (10% Undecylenic Acid), 0.54 OZ (15 g) bottle, Manufact… →
- Blaine Labs Inc — Class II recall: Fungal Fusion ERADICATION Solution, Antifungal & Antimicrobial Kit. Contains, 1x… →
- Blaine Labs Inc — Class II recall: TRIPENICOL S Antifungal Solution (Undecylenic Acid 25%), 1.25 FL OZ (37.5 mL) bo… →
- Blaine Labs Inc — Class I recall: Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37… →
- Blaine Labs Inc — Class II recall: TERPENICOL Antifungal Solution, (Undecylenic (10-Undecenoic) acid 25%), 1.0 Fl O… →
- Blaine Labs Inc — Class II recall: TRIFLUENT PHARMA TRIDERGEL Wound Care Gel, (Benzalkonium Chloride 0.1%), 1.0 fl… →
- Blaine Labs Inc — Class II recall: Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) pac… →
- Blaine Labs Inc — Class II recall: TERPENICOL Antifungal Cream (Undecylenic Acid 13%), 1.0 oz (28 g) bottles, Manuf… →
Compare with
Two different companies merged onto this page by mistake? Or a name variant missing? Tell us — corrections@argushq.ai
Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder
Verified from FDA.gov · Last updated: Jul 8, 2026Cite this record
Reusing this data in reporting or research? Here’s a ready-made citation.
Argus HQ Research (2026). FDA Enforcement History: Blaine Labs Inc. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/company/blaine-labs-inc
"FDA Enforcement History: Blaine Labs Inc." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/company/blaine-labs-inc.
Argus HQ Research. "FDA Enforcement History: Blaine Labs Inc." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/company/blaine-labs-inc.
@misc{argushq_argushq_ai_company_blaine_labs_inc_2026,
title = {FDA Enforcement History: Blaine Labs Inc},
author = {{Argus HQ Research}},
year = {2026},
publisher = {Digital Empire Holdings LLC},
url = {https://argushq.ai/company/blaine-labs-inc},
note = {Accessed: July 23, 2026}
}Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗

