Recall Ledger

Revitaderm Wound Care Gel recall (Blaine Labs Inc)

DrugClass IOngoing

Summary: Blaine Labs Inc is recalling 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.. Reason: Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp.

What is being 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.

Why

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

How serious is it

Class I is the most serious level: FDA considers there is a reasonable probability that using or being exposed to this product will cause serious health problems or death.

Where it was sold

Nationwide in the USA

How to tell if yours is affected

Lot#: BL3608, Exp. 07/01/28.

What to do

Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.

Recall facts

Recall numberD-0692-2026
CategoryDrug
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass I
StatusOngoing
Recall startedApril 8, 2026
ReportedJuly 8, 2026
CompanyBlaine Labs Inc
Company locationSanta Fe Springs, CA, United States
Initiated byVoluntary: Firm initiated
Quantity1,171 - 1 oz bottles

More recalls from Blaine Labs Inc · all drug recalls · recalls from April 2026

Official FDA record