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Recall Observatory FDA recall evidence

Drug product

Estradiol Vaginal Inserts, USP, 10 mcg, Rx only, packaged in a) 8 count (NDC 68462-711-71) and b) 18 count (NDC 68462-711-88) cartons, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale, Goa India, Manufactured for: Glenmark Pharmaceuticals, Inc., USA Mahwah, NJ

D-0350-2019

December 26, 2018

Class II

Product summary

Firm
Glenmark Pharmaceuticals Inc., USA
Event
Event 81876
Status
Terminated
Classification
Class II
Quantity
96,240 applicators
Official record key
drug-enforcement:D-0350-2019

Official wording

Reason: Defective Delivery System: Customer complaints of malfunctioning plunger of the applicator

Code information: Batch numbers: a) 20180393, exp. date 01/31/2020, 20180424, exp. date 02/29/2020, 20180425, exp. date 02/29/2020, 20180427, exp. date 02/29/2020; b) 20180338, exp. date 12/31/2019, 20180386, exp. date 01/31/2020

Distribution pattern: Product was distributed to 5 retailers and 4 distributors throughout the United States who may have further distributed the recalled product.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Defective Delivery System: Customer complaints of malfunctioning plunger of the applicator