US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 3, 2019 (7 years ago)

Estradiol Vaginal Inserts USP 10 mcg, packaged in box of 8 Vaginal Inserts (with…

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

Why it was recalled

Defective Delivery System: Estradiol Vaginal Inserts USP plunger is not functioning properly.

What was recalled

Estradiol Vaginal Inserts USP 10 mcg, packaged in box of 8 Vaginal Inserts (with disposable applicators), Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Colvale-Bardez, Goa 403 513 India, Manufactured for: Glenmark Pharmaceuticals Inc., Mahwah, NJ 07430 USA, NDC 68462-711-71

Recalling firm
Glenmark Pharmaceuticals Inc., USA
NDC code
68462-711-71
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1340-2019

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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