CLASS II Drug recall · Reported 26 Mar 2025 · FDA Enforcement Report

Cinacalcet Hydrochloride Tablets 30 mg recalled

Slate Run Pharmaceuticals is recalling Cinacalcet Hydrochloride Tablets 30 mg, distributed nationwide in the US. The recall was initiated on 7 Mar 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 07711, Exp 07/2025; 08900, Exp 09/2026; 08899, Exp 09/2026
Quantity recalled56,790 bottles

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-0278-2025
FDA event ID
96433
Recalling firm
Slate Run Pharmaceuticals, Columbus, OH
Classification
Class II
Status
Completed
Recall initiated
7 Mar 2025
FDA classified
17 Mar 2025
Reported
26 Mar 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Nitrosamine Impurity

Timeline

7 Mar 2025Recall initiated by company
17 Mar 2025Classified by FDA+10 days
26 Mar 2025Published in enforcement report+9 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: The presence of nitrosamine impurity above the acceptable daily intake limits.

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 Hydrochloride Tablets 30 mg, 30-count bottle, Rx only, Distr. by: Slate Run Pharma., LLC, Columbus, Ohio 43215, Mfg. by: Piramal Pharma Limited, Madhya Pradesh, India, NDC 70436-007-04

Where it was distributed

Product was distributed to 8 distributors who may have further distribute the product nationwide.

Nationwide

Questions about this recall

Why was it recalled?

CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.

Which lots are affected?

Lot # 07711, Exp 07/2025; 08900, Exp 09/2026; 08899, Exp 09/2026

Where was it sold?

Product was distributed to 8 distributors who may have further distribute the product 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

1 other product · FDA event 96433

This product is part of a recall event; the main page for the event is Cinacalcet Hydrochloride Tablets 60 mg recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IICinacalcet Hydrochloride Tablets 60 mg recalledSlate Run PharmaceuticalsNitrosamine ImpurityNationwide

More recalls from Slate Run Pharmaceuticals

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DrugCLASS IIIEptifibatide Injection, 75 mg/ vial recalledEptifibatideSlate Run PharmaceuticalsOtherNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets 60 mg recalledSlate Run PharmaceuticalsNitrosamine ImpurityNationwide

Other Cinacalcet recalls

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