Teva North America recalls Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, Manufactured in Israel by: TEVA
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Failed Tablet/Capsule Specifications
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Source Page by GovInfoNow · govinfonow.com/recall/42608-teva-north-america-recalls-divalproex-sodium-delayed-release-tablets-usp · Recall date May 18, 2016 · FDA enforcement record: FDA #D-1449-2016
Cite this page
“Teva North America recalls Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, Manufactured in Israel by: TEVA.” GovInfoNow, recall dated May 18, 2016. https://govinfonow.com/recall/42608-teva-north-america-recalls-divalproex-sodium-delayed-release-tablets-usp. Based on FDA recall #D-1449-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1449-2016%22&limit=1).
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Contact Teva North America
We’ve drafted a message you can send Teva North America to request your refund or repair — edit it as you like.
Subject: Recall D-1449-2016 — Teva North America Teva North America recalls Divalproex Sodium Delayed-release Tablets USP, RX, 25 Hello, I own a Teva North America recalls Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg, 100 count bottles, Manufactured in Israel by: TEVA that is covered by recall D-1449-2016 from Teva North America. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-1449-2016 (May 18, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1449-2016 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.