Blaine Labs Inc recalls Revitaderm Wound Care Gel
- Recalling company
- Blaine Labs Inc
- Product
- 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
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Apr 8, 2026
- Reported
- Jul 8, 2026
- Distribution
- Nationwide in the USA
- Status
- Ongoing
- Quantity
- 1,171 - 1 oz bottles
- Lot / codes
- Lot#: BL3608, Exp. 07/01/28.
- Company location
- Santa Fe Springs, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0692-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0692-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.