Teva Recalls Terazosin HCl 10mg Capsules Due to Labeling Error
Teva recalls 6,267 bottles of Terazosin Hydrochloride 10mg capsules because the label incorrectly states 10mg while containing 5mg. Check your lot number.
Use caution until it’s fixed
Labeling -label error on declared strength: unopened, sealed bottle of Terazosin Hydrochloride (HCl) 10mg Capsules contained Terazosin HCl 5 mg Capsules
Contact the company
What happened, in plain English
Teva Pharmaceuticals USA is recalling a specific lot of Terazosin Hydrochloride Capsules because the bottle label declares a strength of 10 mg, but the contents are actually 5 mg capsules. This labeling error affects 6,267 bottles distributed nationwide and in Puerto Rico. The record does not specify any reported injuries or provide a remedy for consumers. Read more at govinfonow.com/recall/46828-teva-pharmaceuticals-usa-inc-recalls-terazosin-hydrochloride-capsules-10-mg.
Source Summary by GovInfoNow · govinfonow.com/recall/46828-teva-pharmaceuticals-usa-inc-recalls-terazosin-hydrochloride-capsules-10-mg · Updated October 13, 2026 · FDA enforcement record: FDA #D-842-2013
Cite this page
“Teva Recalls Terazosin HCl 10mg Capsules Due to Labeling Error.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/46828-teva-pharmaceuticals-usa-inc-recalls-terazosin-hydrochloride-capsules-10-mg. Based on FDA recall #D-842-2013 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-842-2013%22&limit=1).
Why it’s dangerous
The hazard is a discrepancy between the labeled strength (10 mg) and the actual content (5 mg). Taking less medication than prescribed may result in inadequate treatment for the condition Terazosin is used to manage, such as high blood pressure or urinary retention. The record does not describe specific injury mechanisms beyond this dosage mismatch.
Who’s affected
Patients who have been prescribed Terazosin Hydrochloride 10 mg capsules from Teva Pharmaceuticals USA, specifically those with lot number N07321 and expiration date 6/14. Individuals in the United States and Puerto Rico who purchased these bottles are at risk of receiving the incorrect dosage.
How to tell if you have this one
Check your bottle for the brand Teva Pharmaceuticals USA and the product name Terazosin Hydrochloride Capsules, 10 mg. Verify that the NDC is 0093-4339-01, the lot number is N07321, and the expiration date is 6/14. The bottles are 100-count sizes.
- Brand
Teva Pharmaceuticals- Category
Drug
What to do — step by step
Check your bottle details
Verify if your bottle matches the recalled lot number N07321 and expiration date 6/14.
Contact your pharmacy or doctor
Since no remedy is stated in the record, consult your healthcare provider for guidance on how to proceed with this specific lot.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide and Puerto Rico” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 13 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-842-2013 (July 23, 2013) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-842-2013 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 13, 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.