February 2016 FDA Recall Drug by Teva Pharmaceuticals Usa
D-0774-2016 - Failed Impurities/Degradation Specifications

This Class II drug recall was voluntarily initiated by Teva Pharmaceuticals Usa on February 5, 2016 for the product Drug. The FDA reported the reason for recall as failed impurities/degradation specifications. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-0774-2016

Reason for Recall
Failed Impurities/Degradation Specifications: Out of specification test results for impurities during stability testing.
Initiated
02-05-2016
Reported
03-23-2016
Quantity
30,891 Bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Teva Pharmaceuticals USA
Nationwide and Puerto Rico
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.

Batch or Lot Expiration Information

Lot# : 13013.009A, Exp. 02/2016