Class III
Terminated
Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02
- Company
- Impax Laboratories, Inc.
- Recall Initiated
- March 17, 2016
- Posted
- April 20, 2016
- Recall Number
- D-0820-2016
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 28,001 HDPE bottles (14,000,500 capsules)
- Firm Location
- Hayward, CA, United States
Reason for Recall
Labeling: Incorrect or Missing Lot and/or Exp. Date
Distribution
Nationwide
Lot / Code Info
Lot # 10008624, 10008831; Exp. 10/16 Lot # 10009339; Exp. 02/17 Lot # 10009566,10009627; Exp. 04/17 Lot # 10010200, 20001419A, 20001426A; Exp. 10/17 Lot # 20001732A; Exp. 04/18 Lot # 20001790A, 20001791A, 20001792A; Exp. 05/18
More recalls by Impax Laboratories, Inc.
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