Home / Recalls / Sandoz Incorporated / D-0943-2017

D-0943-2017 Class III Terminated

Recalled by Sandoz Incorporated — Broomfield, CO

Recall Details

Product Type: Drugs
Report Date: July 12, 2017
Initiation Date: June 16, 2017
Termination Date: January 14, 2019
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 38,234 bottles

Product Description

Amitriptyline HCl Tablets, USP 25 mg, Packaged in a)100-count bottles (NDC 0781-1487-01) and b) 1000-count bottles ( NDC 0781-1487-10), Rx only, Manufactured by Sandoz Inc., Princeton, NJ 08540

Reason for Recall

Cross Contamination With Other Product: Imipramine

Distribution Pattern

Product was distributed throughout the United States

Code Information

Lot #: a) GR3831, GS9690, Exp. 08/2019; b) GR3832, Exp. 08/2019.

Other recalls by Sandoz Incorporated

D-0631-2018 Class III — Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles (April 6, 2018)
D-0236-2017 Class II — Nadolol Tablets, USP, 40mg, packaged in 1000-count bottle, Rx Only, Manufactured (December 22, 2016)
D-0291-2015 Class III — Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz (December 5, 2014)
D-1509-2014 Class II — Alprazolam Tablets, USP, 0.25mg, Rx only, 1000 tablets, Sandoz Inc., Princeton, (July 25, 2014)
D-383-2014 Class II — Tacrolimus Capsules, USP, 0.5 mg, 100 capsules/bottle, Rx only, Manufactured in (October 22, 2013)
D-66373-001 Class III — Hydroxychloroquine Sulfate Tablets, USP, 200 mg, Rx Only, 100 Tablets per bottle (September 25, 2013)
D-854-2013 Class III — Introvale (levonorgestrel and ethinyl estradiol) tablets, USP, 0.15 mg/0.03 mg, (August 7, 2013)
D-805-2013 Class II — Estarylla (Norgestimate and Ethinyl Estradiol) Tablets. USP, 0.25mg/0.035mg, 3X2 (June 21, 2013)
D-597-2013 Class II — Cefazolin, injection, 1 gram per vial, 25 vials per box, sterile, Rx only, singl (May 30, 2013)
D-832-2013 Class I — Methotrexate Injection, USP, Preservative-Free, 1 g/40 mL (25 mg/mL), 40 mL Sing (May 20, 2013)