Recall details are shown for all drugs with the same active ingredient as the chosen drug. Please read the Product Description carefully and consult the distribution map to determine if the recall effects you.
Product Description: alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0068-1.
Product Quantity: 6,789 bottles
Identifiers: Lot # EH8348, exp. date August 2023
Recall Reason: Failed Dissolution Specifications: low out-of-specification dissolution test results observed.
Initiation Date: 04/28/2022 • Recall Number: D-0844-2022
Report Date: 05/11/2022 • Reporting Firm: Viatris Inc
Product Description: Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-3086-06, UPC 3 0228-3086-06 2.
Product Quantity: 5,148 bottles
Identifiers: Lot #: 57617531, Exp 03/14
Recall Reason: Failed Dissolution Specifications: Product did not meet specification requirements for dissolution.
Initiation Date: 02/04/2014 • Recall Number: D-1091-2014
Report Date: 03/12/2014 • Reporting Firm: Actavis Elizabeth LLC
Product Description: Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY ACTAVIS ELIZABETH LLC., Elizabeth, NJ, NDC 0228-4025-11
Product Quantity: 756 bottles
Identifiers: Lot # 59380831, Exp. May 2014
Recall Reason: Failed Tablet/Capsule Specifications; partial tablet erosion resulting in tablet weights below specification in some tablets
Initiation Date: 10/09/2013 • Recall Number: D-018-2014
Report Date: 12/04/2013 • Reporting Firm: Actavis Elizabeth LLC
Product Description: Xanax (alprazolam) tablets, 0.25 mg, 100-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co. Division of Pfizer Inc, NY, NY 10017, NDC 0009-0029-01
Product Quantity: 21,120 HDPE bottles
Identifiers: Lot # C111054; Exp. 02/16
Recall Reason: Subpotent Drug
Initiation Date: 09/24/2015 • Recall Number: D-0161-2016
Report Date: 11/04/2015 • Reporting Firm: Pfizer Inc.
Product Description: Alprazolam tablets, USP, CIV, 0.25 mg, Rx Only, a) 500 count bottle, b) 1000 count bottle, Distributed by: Greenstone LLC, Peapack, NJ, 07977, a) NDC 59762-3719-3, b) NDC 59762-3719-4.
Product Quantity: 12,310 bottles
Identifiers: Lot #: a) C100429, Exp 03/15, b) C120293, Exp 01/17
Recall Reason: Subpotent Drug
Initiation Date: 12/17/2014 • Recall Number: D-0326-2015
Report Date: 12/31/2014 • Reporting Firm: Neolpharma, Inc.
Product Description: Alprazolam Tablets, USP, 0.25mg, Rx only, 1000 tablets, Sandoz Inc., Princeton, NJ --- NDC 0781-1061-10
Product Quantity: 1,332 bottles
Identifiers: Lot EJ9591
Recall Reason: Presence of Foreign Substance; tablets may contain stainless steel metal particulates
Initiation Date: 07/25/2014 • Recall Number: D-1509-2014
Report Date: 08/06/2014 • Reporting Firm: Sandoz Incorporated
Product Description: Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 07207 USA, NDC 0228-2031-50
Product Quantity: 9447 Bottles
Identifiers: Lot # 1826E131, Exp 04/2015
Recall Reason: Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg.
Initiation Date: 02/10/2014 • Recall Number: D-1153-2014
Report Date: 03/19/2014 • Reporting Firm: Actavis Elizabeth LLC