Product Safety Recalls

Product Recall Tracker

Recall D-0891-2022

Description: Losartan Potassium & HCTZ Tablets 50mg/12.5 mg, hydrochlorothiazide USP 12.5, Pkg Size: 90, NDC: 68788-7758-09.

Recall D-0891-2022 Information

Mandated?Voluntary: Firm initiated
Recall NumberD-0891-2022
Event ID90148
DistributionWithin the U.S in FL and CA.
Quantity31 bottles of 90 tables (Lot: K1721D); 5 bottles of 90 tablets (K1021E).
Recall ReasonCGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Drug ClassificationClass II
Drug Code Info20220601
Recall Initiation Date20220503
Report Date20220601
Classification Date20220524
Address1250 N Lakeview Ave Ste O
Anaheim, CA 92807-1801
United States
Recalling FirmPreferred Pharmaceuticals, Inc.
Initial Notification Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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