US Drug Recall Register
Class I · High risk Ongoing Initiated Apr 8, 2026 (5 months ago)

Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL)…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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

What was recalled

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.

Recalling firm
Blaine Labs Inc
NDC code
63347-120-02
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0692-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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