Lantiseptic recalls

The FDA has published 2 recalls involving Lantiseptic since 2025. The latest was reported on 26 Nov 2025. Most were for manufacturing (cgmp) deviations. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls2since 2025

Last 12 months2reported

Class I00% of total

Ongoing2latest 26 Nov 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 2 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 2 100%Class III 0 0%

Why lantiseptic is recalled

Manufacturing (CGMP) Deviations2100%

Companies

DermaRite Industries2100%

By year

20252100%

Ongoing lantiseptic recalls

2 active

Reported	Class	Recall	Company	Reason	Where
26 Nov 2025Drug	CLASS II	Lantiseptic, Dry Skin Therapy, Lanolin recalled by DermaRite Industries	DermaRite Industries	Manufacturing (CGMP) Deviations	Nationwide
26 Nov 2025Drug	CLASS II	Lantiseptic, Skin Protectant, Lanolin recalled by DermaRite Industries	DermaRite Industries	Manufacturing (CGMP) Deviations	Nationwide

All lantiseptic recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
26 Nov 2025Drug	CLASS II	Lantiseptic, Dry Skin Therapy, Lanolin recalled by DermaRite Industries	DermaRite Industries	Manufacturing (CGMP) Deviations	Nationwide
26 Nov 2025Drug	CLASS II	Lantiseptic, Skin Protectant, Lanolin recalled by DermaRite Industries	DermaRite Industries	Manufacturing (CGMP) Deviations	Nationwide

Should you stop taking Lantiseptic?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.