US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Oct 23, 2024 (2 years ago)

Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for…

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

Why it was recalled

Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.

What was recalled

Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Exelan Pharmaceuticals, NDC 76282-0478-90

Recalling firm
Cipla USA, Inc.
NDC code
76282-0478-90
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0044-2025

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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