Teva Pharmaceuticals USA recalls Clonazepam Orally Disintegrating Tablets USP, 2 mg., 60-count carton. RX only. Teva Pharmaceuticals USA, INC. North
Teva Pharmaceuticals recalls 2mg Clonazepam orally disintegrating tablets due to water content failure in stability testing. This affects RX-only products with specific lot numbers.
Lower-risk recall
Failed Stability Specifications: Out-of-specification test result for water content obtained during routine stability testing.
Contact the company & request your remedy
What happened, in plain English
Teva Pharmaceuticals is recalling 2mg Clon: 60-count orally disintegrating tablets because they failed stability testing for water content. This means the medication may not be safe for use as intended. Read more at govinfonow.com/recall/39559-teva-clonazepam-tablets-recall-water-content-issue.
Source Summary by GovInfoNow · govinfonow.com/recall/39559-teva-clonazepam-tablets-recall-water-content-issue · Updated October 6, 2026 · FDA enforcement record: FDA #D-0082-2019
Cite this page
“Teva Clonazepam Tablets Recall: Water Content Issue.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39559-teva-clonazepam-tablets-recall-water-content-issue. Based on FDA recall #D-0082-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0082-2019%22&limit=1).
Why it’s dangerous
The tablets failed stability testing for water content, which could mean the medication is less effective or unsafe. This issue occurs during routine testing and does not indicate immediate danger to users.
Who’s affected
Prescription medication users who have the specific lot number 34033752A of the 2mg Clonazepam tablets. People with seizure disorders or anxiety conditions that require this medication are most at risk.
How to tell if you have this one
Check for the lot number 34033752A on the packaging. The product is a 2mg Clonazepam orally disintegrating tablet in a 60-count carton, sold under Teva Pharmaceuticals USA.
- Brand
Teva Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Details
Look for the lot number 34033752A on the packaging of the 2mg Clonazepam orally disintegrating tablets.
Questions people ask
Is this medication safe to use?
The recall is due to water content failure in stability testing, but the medication is still safe for use as intended unless the specific lot number is affected.
What should I do if I have the recalled product?
The recall record does not specify a remedy, so no action is required beyond checking the lot number.
How can I confirm if my product is recalled?
Check the lot number 34033752A on the packaging of the 2mg Clonazepam orally disintegrating tablets.
Contact Teva Pharmaceuticals
We’ve drafted a message you can send Teva Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0082-2019 — Teva Pharmaceuticals Teva Pharmaceuticals Hello, I own a Teva Pharmaceuticals that is covered by recall D-0082-2019 from Teva Pharmaceuticals. 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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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-0082-2019 (September 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0082-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.