Telmisartan and Amlodipine
Superpotent Drug: potential for the Telmisartan content in these lots to exceed specifications
Recall notice
Superpotent Drug: potential for the Telmisartan content in these lots to exceed specifications
We’re still writing up this recall
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
Source Page by GovInfoNow · govinfonow.com/recall/1927668-viatris-inc-recalls-telmisartan-and-amlodipine-tablets-usp-40mg-5 · Recall date October 1, 2026 · FDA enforcement record: FDA #D-0049-2027
Cite this page
“Telmisartan and Amlodipine.” GovInfoNow, recall dated October 1, 2026. https://govinfonow.com/recall/1927668-viatris-inc-recalls-telmisartan-and-amlodipine-tablets-usp-40mg-5. Based on FDA recall #D-0049-2027 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0049-2027%22&limit=1).
How to tell if you have this one
- Brand
Viatris, Inc.- Category
Drug
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “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 published this recall 27 days after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
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-0049-2027 (October 1, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0049-2027 to see it in context.
- 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.