US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Nov 5, 2025 (10 months ago)

Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective container - seal not adhering to bottles

What was recalled

Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09.

Recalling firm
Lupin Pharmaceuticals Inc.
NDC code
68180-353-09
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0227-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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