CLASS II ONGOING Drug recall · Reported 1 Jul 2026 · FDA Enforcement Report

Sensipar (cinacalcet) Tablets, 30mg recalled by Amgen

Amgen is recalling Sensipar (cinacalcet) Tablets, 30mg, distributed nationwide in the US. The recall was initiated on 4 Jun 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot#: 1156858, Exp. Date 12/31/2027.
NDC55513-073, 55513-074, 55513-075
Quantity recalled9565 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-0613-2026
FDA event ID
99077
Recalling firm
Amgen, Thousand Oaks, CA
Manufacturer
Amgen Inc
Classification
Class II
Status
Ongoing
Recall initiated
4 Jun 2026
FDA classified
23 Jun 2026
Reported
1 Jul 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

4 Jun 2026Recall initiated by company
23 Jun 2026Classified by FDA+19 days
1 Jul 2026Published in enforcement report+8 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

Product as listed by the FDA

Sensipar (cinacalcet) Tablets, 30mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-073-30

Where it was distributed

Nationwide within the United States

Nationwide

Questions about this recall

Is Sensipar (cinacalcet) Tablets, 30mg recalled?

Yes. Amgen recalled Sensipar (cinacalcet) Tablets, 30mg on 4 Jun 2026. The recall is Class II and its status is Ongoing. Recall number D-0613-2026.

Why was it recalled?

CGMP Deviations

Which lots are affected?

Lot#: 1156858, Exp. Date 12/31/2027.

Where was it sold?

Nationwide within the United States

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

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