US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 5, 2016 (11 years ago)

Paricalcitol Capsules, 1 mcg, 30 tablets per Bottle, Rx Only, Manufactured By…

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

Why it was recalled

Failed Impurities/Degradation Specifications: Out of specification test results for impurities during stability testing.

What was recalled

Paricalcitol Capsules, 1 mcg, 30 tablets per Bottle, Rx Only, Manufactured By: Pharmaceutics International, Inc., Hunt Valley, MD 21031, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-7656-56.

Recalling firm
Teva Pharmaceuticals USA
NDC code
0093-7656-56
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0774-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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