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Class IIOngoing

Cinacalcet Tablets recall

FDA recall D-0026-2025 · initiated Oct 9, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Nov 6, 2024How we research

Dr. Reddy's Laboratories, Inc. recalled Cinacalcet Tablets in Oct 2024 — an FDA Class II recall (D-0026-2025) because CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit.

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

Why it was recalled

CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

An impurity above the accepted limit

A by-product of manufacturing or storage exceeded the limit the FDA accepts. Nitrosamines are the common example: the concern is long-term exposure, not immediate danger from one dose.

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# T2200120, T2200121, T2200119, T2200116, T2200118, T2200117, Exp 11/2024; T2200695, T2200694, T2200696, T2200697, Exp 01/2025; T2201426, T2201428, T2201432, T2201427, T2201430, T2201429, T2201431, Exp 03/2025; T2202743, T2202742, T2202741, & T2202740, Exp 06/2025; T2203081, T2203079, T2203080, T2203082, T2203083 & T2203084, Exp 07/2025; T2300770, T2300771, T2300769, T2300766, T2300767 & T2300768, Exp 12/2025 Lots T2301663, T2301665, T2301662, T2301664, T2301667, T2301661, T2301666, T2301660, T2301658 & T2301659, Exp Date 02/2026 Lots T2304704, T2304703, T2304705, T2304706, Exp Date 08/2026 Lots T2400468, T2400469, T2400473 & T2400474 Exp Date 11/2026

Quantity recalled: 285126 bottles

Details

Product
Cinacalcet Tablets, 30 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India, NDC 43598-367-30.
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
USA Nationwide.
Initiated
Oct 9, 2024
FDA report date
Nov 6, 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 Cinacalcet Tablets recalled?
Dr. Reddy's Laboratories, Inc. recalled Cinacalcet Tablets in Oct 2024 — an FDA Class II recall (D-0026-2025) because CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Cinacalcet Tablets recalled?
Per the FDA enforcement record, the reason for recall D-0026-2025 was: CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
Is a recalled Cinacalcet 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 Cinacalcet Tablets are affected?
Distributed: USA Nationwide.. The recall covers these lots — Lot# T2200120, T2200121, T2200119, T2200116, T2200118, T2200117, Exp 11/2024; T2200695, T2200694, T2200696, T2200697, Exp 01/2025; T2201426, T2201428, T2201432, T2201427, T2201430, T2201429, T2201431, Exp 03/2025; T2202743, T2202742, T2202741, & T2202740, Exp 06/2025; T2203081, T2203079, T2203080, T2203082, T2203083 & …. 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-0026-2025.

Source: openFDA Drug Enforcement record D-0026-2025

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