Use caution Drug recall · FDA · Published October 27, 2021

Teva Recalls Cartia XT 120 mg Due to Wrong Expiration Date

Teva Pharmaceuticals is recalling specific lots of Cartia XT 120 mg capsules because the label shows an incorrect expiration date. Check your bottle's lot number.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0232-2022Drug Teva ›

Use caution until it’s fixed

Labelling: Incorrect Exp. Date

Take action

Contact the company

Recalling firmTeva Pharmaceuticals USA400 Interpace Pkwy · Parsippany, NJ 07054-1120

✎ GovInfoNow plain-language explainer

Teva Pharmaceuticals USA is recalling 32,316 bottles of Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules) 120 mg because the label displays an incorrect expiration date. The affected product was distributed nationwide in the USA. The recall notice does not specify a remedy or return process for consumers. Read more at govinfonow.com/recall/35581-teva-recalls-cartia-xt-120-mg-due-to-wrong-expiration.

Source Summary by GovInfoNow · govinfonow.com/recall/35581-teva-recalls-cartia-xt-120-mg-due-to-wrong-expiration · Updated October 10, 2026 · FDA enforcement record: FDA #D-0232-2022

Cite this page

“Teva Recalls Cartia XT 120 mg Due to Wrong Expiration Date.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/35581-teva-recalls-cartia-xt-120-mg-due-to-wrong-expiration. Based on FDA recall #D-0232-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0232-2022%22&limit=1).

The FDA announced on 2021-10-27 that Teva Pharmaceuticals USA voluntarily recalled Cartia XT capsules due to incorrect expiration dates on the labeling. The recall affects 32,316 bottles distributed nationwide.

How to tell if you have it

Brand: Teva
Product: Cartia XT Capsules (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg
NDC: 62037-597-90
Lot #: 100023805
Labelled Exp. Date: 05/2023
Quantity: 90 capsules per bottle

The hazard

The recall is classified as Class II due to the hazard of incorrect expiration dates on the product labeling.

Context

GovInfoNow's records show Teva Pharmaceuticals USA has 97 other recalls on record since 2013-10-11. Other recent recalls include Teva Doxylamine Succinate Tablets Recall (2022-01-18), Teva Tretinoin Capsules 10mg Recall (2022-01-10), and Teva Mimvey Tablets Recall (2022-01-07). Other recent recalls of similar products include Teva Isotretinoin Capsules 30mg Recall (2026-01-12), Kirkman Lidocaine Cream Recall (2026-02-18), and OurPharma Fentanyl Injection Recall (2026-09-03).

How to tell if you have this one

Check your bottle for NDC 62037-597-90 and Lot # 100023805. The label should show an expiration date of 05/2023. The product is manufactured by Teva Pharmaceuticals USA, Inc., Parsippany, NJ, or Actavis Laboratories FL. Inc., Fort Lauderdale, FL.

Brand
Teva
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Your Bottle
Verify if your Cartia XT bottle has NDC 62037-597-90 and Lot # 100023805 with an expiration date of 05/2023.
Contact Your Pharmacist
Since the recall record does not list a specific remedy, contact your pharmacy or healthcare provider to discuss replacing the medication or obtaining further instructions.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Distributed Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 14 months after the firm started it.

Oct 27, 2021Firm started the recall
Nov 15, 2021FDA classified it Class II
Nov 24, 2021Published in FDA’s Enforcement Report
Dec 21, 2022FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

How many bottles are being recalled?

Approximately 32,316 bottles of Cartia XT 120 mg are included in this recall.

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Link to this recall

<a href="https://govinfonow.com/recall/35581-teva-recalls-cartia-xt-120-mg-due-to-wrong-expiration">Teva Recalls Cartia XT 120 mg Due to Wrong Expiration Date (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0232-2022 (October 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0232-2022 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.