Class II
Terminated
Losartan Potassium USP, 50 mg, RX Only, Pkg By PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 60 Tablets NDC: 43063-854-60; b) 90 Tablets NDC: 43063-0854-90
- Company
- Pd-Rx Pharmaceuticals, Inc.
- Recall Initiated
- March 8, 2019
- Posted
- May 5, 2021
- Recall Number
- D-0341-2021
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 576 bottles
- Firm Location
- Oklahoma City, OK, United States
Reason for Recall
CGMP deviation: Product found to contain trace amounts of NMBA
Distribution
AK, AZ, CA, CO, FL, KY, MA, MI, MN, NC, OH, OR, WI, WY
Lot / Code Info
Lots: A19B99 Exp. 11/30/2019; B19A26 Exp. 11/30/2019; B19A69 Exp. 11/30/2019; E18F12 Exp.: 09/30/19; F18A12 Exp.: 09/30/19; F18F06 Exp.: 09/30/19; G18B43 Exp.: 09/30/19; G18C43 Exp.: 09/30/19; G18F75 Exp.: 09/30/19; H18D55 Exp.: 09/30/19; I18A11 Exp.: 09/30/19; I18E32 Exp.: 09/30/19; J18A90 Exp.: 09/30/19; J18D50 Exp. 11/30/2019; L18D01 Exp. 11/30/2019
More recalls by Pd-Rx Pharmaceuticals, Inc.
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May 10, 2023 · Class II
Losartan Potassium Tablets, USP 25 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx P...
Jul 6, 2022 · Class II
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