CLASS II Drug recall · Reported 19 Apr 2017 · FDA Enforcement Report

Estriol Micronized, USP, Bulk recalled by Qinhuangdao Zizhu

Qinhuangdao Zizhu Pharmaceutical is recalling Estriol Micronized, USP, Bulk, distributed in Colorado, Minnesota, New Jersey, New York, South Carolina, Texas. The recall was initiated on 24 Mar 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch 81801504002 to 81801701003, exp 4/12/2017 through 1/19/2019
Quantity recalledN/A

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0656-2017
FDA event ID
76890
Recalling firm
Qinhuangdao Zizhu Pharmaceutical, Qinhuangdao, N/A
Classification
Class II
Status
Terminated
Recall initiated
24 Mar 2017
FDA classified
11 Apr 2017
Reported
19 Apr 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

24 Mar 2017Recall initiated by company
11 Apr 2017Classified by FDA+18 days
19 Apr 2017Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

cGMP Deviations; lack of quality assurance.

Product as listed by the FDA

Estriol Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China 44132-007-06

Where it was distributed

Product distributed to NY, TX, SC, CO, MN and NJ

ColoradoMinnesotaNew JerseyNew YorkSouth CarolinaTexas

Questions about this recall

Why was it recalled?

cGMP Deviations; lack of quality assurance.

Which lots are affected?

Batch 81801504002 to 81801701003, exp 4/12/2017 through 1/19/2019

Where was it sold?

Product distributed to NY, TX, SC, CO, MN and NJ

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

6 other products · FDA event 76890

More recalls from Qinhuangdao Zizhu Pharmaceutical

All 7

Other Estriol Micronized recalls

All 2
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIEstriol USP Micronized recalled by Triova PharmaceuticalsTriova PharmaceuticalsPotency & AssayNationwide