Revitaderm Wound Care recall
Blaine Labs Inc recalled Revitaderm Wound Care on July 8, 2026 because of cGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated. It was sold nationwide.
Why it was recalled
CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated
What's recalled
Revitaderm Wound Care, First Aid Antiseptic Gel, Benzalkonium Chloride 0.1%) packaged as (a) 1.0 Fl OZ (16 mL) bottle, long pointy cap, NDC 63347-120-02; (b) 3.0 Fl OZ (85 g) tube, with short twist cap, NDC 63347-120-01; Manufactured By: Blaine Labs, Inc. 11037 Lockport Place, Santa Fe Springs, CA 90670,
Quantity: 5,555 bottles and tubes
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Blaine Labs Inc, Santa Fe Springs, CA
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Nationwide in the USA - Status
- Ongoing
- Recall number
- D-0699-2026
- Source
- U.S. Food and Drug Administration
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