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Class IIOngoing

Lanthanum Carbonate Chewable Tablets recall

FDA recall D-0044-2025 · initiated Oct 23, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Nov 20, 2024How we research

Cipla USA, Inc. recalled Lanthanum Carbonate Chewable Tablets in Oct 2024 — an FDA Class II recall (D-0044-2025) because Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

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

The manufacturing process itself

The FDA found the process itself out of compliance, usually before any defective product was identified.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot# NB240873, Exp 03/31/2026

Quantity recalled: N/A

Details

Product
Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Exelan Pharmaceuticals, NDC 76282-0478-90
Recalling company
Cipla Limited
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
USA nationwide.
Initiated
Oct 23, 2024
FDA report date
Nov 20, 2024
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Lanthanum Carbonate Chewable Tablets recalled?
Cipla USA, Inc. recalled Lanthanum Carbonate Chewable Tablets in Oct 2024 — an FDA Class II recall (D-0044-2025) because Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Lanthanum Carbonate Chewable Tablets recalled?
Per the FDA enforcement record, the reason for recall D-0044-2025 was: Failed Tablet/Capsule Specifications: Complaints received of crushed and broken tablets.
Is a recalled Lanthanum Carbonate Chewable Tablets dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Lanthanum Carbonate Chewable Tablets are affected?
Distributed: USA nationwide.. The recall covers these lots — Lot# NB240873, Exp 03/31/2026. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0044-2025.

Source: openFDA Drug Enforcement record D-0044-2025

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