FreshRecalls

⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a very recent recall may be missing. Everything shown is accurate as of the last checked time on this page — for anything time-critical, confirm with the official sources linked below.

FDAClass I · Drug · Recalled July 8, 2026

Revitaderm Wound Care Gel recall — Blaine Labs Inc

Hazard: Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp

Class I: most serious — reasonable probability of serious health consequences or death.

View the official FDA enforcement record (openFDA) ↗

Official recall ID
D-0692-2026
Brand
Blaine Labs
Classification
Class I
Units affected
1,171 - 1 oz bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Description

Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL) bottle, shorter twist cap, Manufactured By: Blaine Labs, Inc. 11037 Lockport Place Santa Fe Springs, CA 90670, NDC 63347-120-02.

Affected products

Companies & origin

Recalling firm location
Santa Fe Springs, CA, United States
Firm address
11037 Lockport Pl, N/A, 90670-4634

Identifying details (verbatim from the notice)

Product codes / lots
Lot#: BL3608, Exp. 07/01/28.
Distribution
Nationwide in the USA
Firm notified the public via
Press Release
FDA event ID
98731
Recall initiated
April 8, 2026
FDA classified
July 16, 2026
FDA report date
July 8, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 23, 2026 at 11:04 PM UTC.

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