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Home › FDA recalls › Lidocaine Ointment USP
CLASS II · ModerateFDA

Direct Rx recalls Lidocaine Ointment USP

📅 Sep 29, 2026 · 📍 Nationwide
Recalling company
Direct Rx
Product
Lidocaine Ointment USP, 5.0 % 50g JAR, Rx only, Packaged and Distributed by: Direct Rx Dawsonville, GA 30534, NDC 72189-0211-50
Reason
Subpotent Drug
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Sep 29, 2026
Reported
Nov 4, 2026
Distribution
Nationwide within the United States
Status
Ongoing
Quantity
493 jars
Lot / codes
LOT#: 03AP2511, 30AP2518, 18JU2519, 18JU2520, Exp. Date 04/30/2027.
Company location
Dawsonville, GA
Recall type
Voluntary: Firm initiated
Recall number
D-0107-2027
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number D-0107-2027 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.