Is Pyrazinamide recalled?

3 FDA recalls mention Pyrazinamide. The most recent are listed below.

Recalls are matched by product description. A recall usually affects specific lots, not every package of Pyrazinamide.

Class II · Moderate risk Ongoing May 1, 2023

Pyrazinamide, 500 mg Tablet, packaged in a) 29 x 30-count card, NDC # 70518-2534-01; b) 1 x 100 UD box, NDC # 70518-2534-00…

Reason CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity…

RemedyRepack Inc. NDC 70518-2534-01 D-0578-2023

Class II · Moderate risk Terminated Feb 15, 2022

Pyrazinamide Tablets, USP 500 mg, 100-count bottles, Rx only, Manufactured by: ULTRAtab Laboratories, Inc. Highland, NY 12528…

Reason cGMP Deviations

ANI Pharmaceuticals, Inc. NDC 67253-660-10 D-0568-2022

Class II · Moderate risk Terminated Nov 14, 2014

Pyrazinamide active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front…

Reason Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they…

Attix Pharmaceuticals D-871-2015

Pyrazinamide, 500 mg Tablet, packaged in a) 29 x 30-count card, NDC # 70518-2534-01; b) 1 x 100 UD box, NDC # 70518-2534-00…

Pyrazinamide Tablets, USP 500 mg, 100-count bottles, Rx only, Manufactured by: ULTRAtab Laboratories, Inc. Highland, NY 12528…

Pyrazinamide active pharmaceutical ingredient packaged in varying grams or kg in bags or drums, Attix Pharmaceuticals, 184 Front…

Get an alert if your medication is recalled