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Drug recall · FDA · Published August 24, 2018

Akorn, Inc. recalls Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx only, Mfg For VersaPharm Incorporated, Maroerre, GA

Failed Impurities/Degradation Specifications: Out of specification (OOS) results for unspecified impurity.

🇺🇸 FDA recall #D-1183-2018DrugAkorn, Inc. ›
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Recalling firmAkorn, Inc.1925 W Field Ct Ste 300, N/A · Lake Forest, IL 60045-4862
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
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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/39682-akorn-inc-recalls-ethosuximide-capsules-usp-250-mg-100-capsules · Recall date August 24, 2018 · FDA enforcement record: FDA #D-1183-2018

Cite this page

“Akorn, Inc. recalls Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx only, Mfg For VersaPharm Incorporated, Maroerre, GA.” GovInfoNow, recall dated August 24, 2018. https://govinfonow.com/recall/39682-akorn-inc-recalls-ethosuximide-capsules-usp-250-mg-100-capsules. Based on FDA recall #D-1183-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1183-2018%22&limit=1).

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  • Brand
    Akorn, Inc.
  • Category
    Drug
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Contact Akorn, Inc.

We’ve drafted a message you can send Akorn, Inc. to request your refund or repair — edit it as you like.

Subject: Recall D-1183-2018 — Akorn, Inc. Akorn, Inc. recalls Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx onl

Hello,

I own a Akorn, Inc. recalls Ethosuximide Capsules, USP, 250 mg, 100 capsules per bottle, Rx only, Mfg For VersaPharm Incorporated, Maroerre, GA that is covered by recall D-1183-2018 from Akorn, Inc..

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-1183-2018 (August 24, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1183-2018 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA