CLASS II ONGOING Drug recall · Reported 11 Dec 2024 · FDA Enforcement Report

Cinacalcet Tablets, 90 mg recalled by Aurobindo Pharma USA

Aurobindo Pharma USA is recalling Cinacalcet Tablets, 90 mg, distributed nationwide in the US. The recall was initiated on 7 Nov 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: a) CFSC23001A, CFSC23001B, Exp 03/31/2025; b) P2300195, Exp 12/31/2024

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0079-2025
FDA event ID
95730
Recalling firm
Aurobindo Pharma USA, East Windsor, NJ
Classification
Class II
Status
Ongoing
Recall initiated
7 Nov 2024
FDA classified
29 Nov 2024
Reported
11 Dec 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Nitrosamine Impurity

Timeline

7 Nov 2024Recall initiated by company
29 Nov 2024Classified by FDA+22 days
11 Dec 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Nitrosamines are impurities that can form during drug manufacturing or storage. Above the FDA acceptable intake limit, long-term exposure may raise cancer risk. The FDA advises patients to keep taking the medicine until they have a replacement.

Product as listed by the FDA

Cinacalcet Tablets, 90 mg, packaged in: a) 30-count HDPE bottle (NDC 65862-833-30), b) 500-count HDPE bottle (NDC 65862-833-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India. 90 mg - 30 Tablets - NDC 65862-833-30 90 mg - 500 Tablets - NDC 65862-833-05

Where it was distributed

USA Nationwide

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot #: a) CFSC23001A, CFSC23001B, Exp 03/31/2025; b) P2300195, Exp 12/31/2024

Where was it sold?

USA Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 95730

This product is part of a recall event; the main page for the event is Cinacalcet Tablets, 60mg recalled by Aurobindo Pharma USA.

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