Akorn recalls all Acyclovir Oral Suspension (200mg/5mL) due to stability concerns after the manufacturer closed. This prescription medication may not be safe for long-term use.
CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Akorn has recalled all prescription Acyclovir Oral Suspension (200mg/5mL) because the manufacturer went out of business and can no longer ensure the product's stability. This means the medication might not be safe to use long-term.
The manufacturer went out of business and can no longer conduct stability studies to ensure the medication remains safe and effective over time. This could lead to potential safety issues if the product is used beyond its intended shelf life.
Prescription patients using Acyclovir Oral Suspension (200mg/5mL) from Akorn. Those with ongoing treatment needs are most at risk if they continue using the product.
Check for the product name 'Acyclovir Oral Suspension' with strength 200mg/5mL. All NDCs and all lots are affected. This is a prescription medication distributed by Akorn Operating Company LLC.
Look for the product name 'Acyclovir Oral Suspension' with strength 200mg/5mL on the label.
The recall states the manufacturer can no longer ensure stability, so it may not be safe for long-term use. Consult your doctor if you have ongoing treatment needs.
The recall does not specify a stop-use instruction, but the manufacturer's closure means the product may not be safe long-term. Contact your doctor for guidance.
The recall record does not mention any replacement options or remedies.
We’ve drafted a message you can send Akorn to request your refund or repair — edit it as you like.
Subject: Recall D-0782-2023 — Akorn Akorn Hello, I own a Akorn that is covered by recall D-0782-2023 from Akorn. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.