Akorn, Inc. recalls RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42.
Failed Impurity/Degradation Specifications: Out of Specifications result obtained for a known impurity.
Recall notice
Failed Impurity/Degradation Specifications: Out of Specifications result obtained for a known impurity.
Contact the company & request your remedy
We’re still writing up this recall
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/43824-akorn-inc-recalls-rifampin-for-injection-usp-600-mg-vial · Recall date August 20, 2015 · FDA enforcement record: FDA #D-0231-2016
Cite this page
“Akorn, Inc. recalls RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42..” GovInfoNow, recall dated August 20, 2015. https://govinfonow.com/recall/43824-akorn-inc-recalls-rifampin-for-injection-usp-600-mg-vial. Based on FDA recall #D-0231-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0231-2016%22&limit=1).
How to tell if you have this one
- Brand
Akorn, Inc.- Category
Drug
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-0231-2016 — Akorn, Inc. Akorn, Inc. recalls RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Hello, I own a Akorn, Inc. recalls RIFAMPIN FOR INJECTION USP, 600 mg*/vial, Rx Only. Mfd. for: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-151-42. that is covered by recall D-0231-2016 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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-0231-2016 (August 20, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0231-2016 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.
