Teva Pharmaceuticals USA recalls Cartia XT 12:00 mg capsules with incorrect expiration dates. Consumers should check labels for exp date 05/2023 and contact Teva for details.
Labelling: Incorrect Exp. Date
Teva Pharmaceuticals USA is recalling Cartia XT 120 mg extended-release capsules that have incorrect expiration dates. This could lead to using expired medication, which might not be safe or effective.
The capsules have an incorrect expiration date printed on the label. This means the medication might be expired and less effective or unsafe for use.
Prescription holders of Cartia XT 120 mg capsules with the label showing expiration date 05/2023 are affected. Most at risk are individuals who take this medication regularly.
Check the label for the expiration date 05/2023. The product is labeled as (a) with NDC 62037-597-90 and lot number 100023805.
Look for the expiration date 05/2023 on the label of the Cartia XT 120 mg capsules.
The recall is for incorrect expiration dates, not a safety hazard. Using expired medication may be less effective but is not immediately dangerous.
Check the label for expiration date 05/2023, NDC 62037-597-90, and lot number 100023805.
The recall does not require immediate action. Check the label and contact Teva Pharmaceuticals USA for further instructions.
We’ve drafted a message you can send Teva Pharmaceuticals USA to request your refund or repair — edit it as you like.
Subject: Recall D-0232-2022 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA Hello, I own a Teva Pharmaceuticals USA that is covered by recall D-0232-2022 from Teva Pharmaceuticals USA. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.