Product Safety Recalls

Product Recall Tracker

Recall D-0886-2022

Description: Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original NDC # 68180-0217-09

Recall D-0886-2022 Information

Mandated?Voluntary: Firm initiated
Recall NumberD-0886-2022
Event ID90127
DistributionProduct was distributed to FL, SC and VA
Quantity26/90 count bottles = 2,340 tablets
Recall ReasonCGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
Drug ClassificationClass II
Drug Code Info20220601
Recall Initiation Date20220502
Report Date20220601
Classification Date20220520
Address625 Kolter Dr Ste 4
Indiana, PA 15701-3571
United States
Recalling FirmRemedyRepack Inc.
Initial Notification Letter
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