“Bionpharma Divalproex Tablets Recall: Foreign Tablets Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/309320-bionpharma-divalproex-tablets-recall-foreign-tablets-risk. Based on FDA recall #D-0742-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0742-2026%22&limit=1).
Bionpharma Inc. recalled Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, distributed nationwide, due to the presence of foreign tablets/capsules, according to the FDA on June 26, 2026.
The recall addresses the presence of foreign tablets/capsules in the product, according to the FDA.
Context
GovInfoNow's records show Bionpharma Inc. has 3 other recalls on record since July 16, 2019. Other recent recalls of similar products include Golden State Baclofen Tablets Recall (Nov. 26, 2025), Amgen Recalls Corlanor 5mg Tablets Due to Foreign Substance (June 4, 2026), and Glenmark Nebivolol Tablets Recall (Nov. 18, 2025).
How to tell if you have this one
Check for the lot number 704C003 on the bottle. The product was made in India and expires December 31, 2028.
Brand
Bionpharma
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the lot number 704C003 on the bottle label.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US 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 33 days after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class II
4Added to GovInfoNow
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-0742-2026 (June 26, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0742-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.