Teva Pharmaceuticals recalls 9mg Budesonide Extended-Release Tablets due to failed dissolution specifications. This may affect medication effectiveness. Contact for return instructions.
“Teva recalls Budesonide 9mg tablets: Failed dissolution specs.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32888-teva-recalls-budesonide-9mg-tablets-failed-dissolution-specs. Based on FDA recall #D-0275-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0275-2024%22&limit=1).
The FDA announced on Jan. 8, 2024, that Teva Pharmaceuticals USA, Inc. voluntarily recalled Budesonide Extended-Release Tablets 9mg due to failed dissolution specifications. The recall affects 10,672 bottles distributed nationwide.
The product failed dissolution specifications, according to the FDA. The recall is classified as Class II.
Context
GovInfoNow's records show Teva Pharmaceuticals USA, Inc. has 59 other recalls on record since April 2, 2012. Other recent recalls of similar products include Novartis Diovan 160mg Tablets (Aug. 4, 2026), AvKARE Rosuvastatin Tablets 10mg (Dec. 31, 2025) and Inventia Chlorthalidone (Sept. 3, 2026).
How to tell if you have this one
Check for the 9mg Budesonide Extended-Release Tablets, 30-count bottle, Rx Only. Look for NDC 0591-2510-30 and lot number 100047273.
Brand
Teva
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Medication Details
Identify the product by checking the NDC code 0591-2510-30 and lot number 100047273.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 30 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-0275-2024 (January 8, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0275-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.