Teva recalls Tri-Lo-Sprintec birth control tablets due to failed dissolution specifications. This may affect product effectiveness. Check NDC 0093-2140-62 and lot numbers for affected items.
“Teva Tri-Lo-Sprintec Tablets Recall: Failed Dissolution Specifications.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32780-teva-tri-lo-sprintec-tablets-recall-failed-dissolution-specifications. Based on FDA recall #D-0428-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0428-2024%22&limit=1).
The FDA announced on March 7, 2024, that Teva Pharmaceuticals USA, Inc. is recalling Tri-Lo-Sprintec tablets due to failed dissolution specifications. The recall affects 92,676 cartons distributed nationwide.
The tablets failed dissolution specifications. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Teva Pharmaceuticals USA, Inc. has 59 other recalls on record since April 2, 2012. Recent Teva recalls include traZODone 50mg tablets recalled on August 24, 2026, for foreign tablet risk, and Octreotide Acetate 30mg Kit recalled on April 24, 2026, due to sterility risks. Other recent recalls of similar products include Viatris Xanax XR 3mg Tablets Recall (March 17, 2026), Novartis Recalls Diovan 160mg Tablets (August 4, 2026), and Inventia Healthcare Chlorthalidone Tablets Recall (June 5, 2026).
How to tell if you have this one
Check for NDC 0093-2140-62 on the packaging. Affected lots include 100039678 (expiring 04/31/2024) and 100038111, 100042277 (expiring 07/31/2024).
Brand
Teva
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for NDC 0093-2140-62 and lot numbers 100039678, 100038111, or 100042277 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “USA nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 12 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
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-0428-2024 (March 7, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0428-2024 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.