Class III
Terminated
Duavee (conjugated estrogens/bazedoxifene) tablets 0.45/20 mg, packaged in 2 blister cards containing 15 tablets each (30 tablets), Rx Only, Distributed by Wyeth Pharmaceuticals LLC A subsidiary of Pfizer In Philadelphia, PA 19101 Made in Ireland, NDC 00008-1123-12
- Company
- Pfizer Inc.
- Recall Initiated
- May 27, 2020
- Posted
- July 1, 2020
- Recall Number
- D-1342-2020
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 544400 packages
- Firm Location
- New York, NY, United States
Reason for Recall
Failed Dissolution Specifications
Distribution
Nationwide within the United States
Lot / Code Info
Lot #: AF7814, 2021 AUG 31; AH6565, 2021 SEP 30, AP5189, 2020 SEP30; CG8921, 2022 FEB 28; CL6603, DH5847, 2022 MAR 31; T17703, T99214 2020 JUN 30, W46878, X07330, 2020 SEP 30; X99074, 2021 JUN 30
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