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Recall Observatory FDA recall evidence

Drug product

Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg, Rx Only, 90 capsules, labelled as (a) Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054; (b) Manufactured By: Actavis Laboratories FL. Inc, Fort Lauderdale FL. 33314 USA, Distributed by Avista Pharma Inc. Parsippany, NJ 07054 USA. NDC 62037-597-90

D-0232-2022

October 27, 2021

Class II

Product summary

Firm
Teva Pharmaceuticals USA
Event
Event 88936
Status
Terminated
Classification
Class II
Quantity
32316 bottles
Official record key
drug-enforcement:D-0232-2022

Official wording

Reason: Labelling: Incorrect Exp. Date

Code information: Lot # 100023805, Exp. Date 05/2023

Distribution pattern: Distributed Nationwide in the USA

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Labelling: Incorrect Exp. Date