Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Ongoing Initiated Jun 4, 2026 (4 months ago)

Sensipar (cinacalcet) (Cinacalcet Hydrochloride)

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations

Cause type: cGMP deviation

Departures from current Good Manufacturing Practice found in production or during FDA inspection. A broad quality-system cause: the batch was made under conditions that fall short of FDA manufacturing standards. All cgmp deviation recalls.

What was recalled

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

Affected NDC 55513-0073-30

Compare with the code on your package — it is the most precise check available.

Drug: Cinacalcet

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Sensipar
cinacalcet hydrochloride
NDC 55513-0073
30 mg/1 Tablet, Coated
Oral
Amgen Inc Rx
Recalling firm
Amgen, Inc.
NDC code
55513-073-30
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0613-2026 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Cinacalcet recalls

See all

Other recalls by Amgen, Inc.

All 2026 recalls