Akorn recalls all Lorazepam Injection vials due to inability to conduct stability studies after the company went out of business. This affects all products manufactured by Akorn, Inc. in Lake Forest, IL.
CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Akorn has recalled all Loraz:epam injection vials because the company went out of business and can no longer perform stability testing. This means the medication may not be safe for use as the manufacturer can no longer ensure its quality.
The company went out of business and can no longer conduct stability studies, which are necessary to ensure the medication remains safe and effective over time. Without this testing, there is a risk that the medication may degrade or become unsafe for use.
Prescription users of Lorazepam injection vials from Akorn, Inc. in Lake Forest, IL. Most at risk are patients who have been prescribed this medication and have not yet received their vials.
Check for vials labeled 'Lorazepam Injection, USP 2 mg/mL, 1 mL vials, Rx Only, Sterile' manufactured by Akorn, Inc. in Lake Forest, IL. All products are affected regardless of lot number or NDC.
Identify the vial label to confirm it matches the recalled product description.
The company went out of business and can no longer continue stability studies, which are necessary to ensure the medication remains safe and effective.
All products manufactured by Akorn, Inc. in Lake Forest, IL are affected, regardless of lot number or NDC.
The recall record does not specify a remedy, so no action is required beyond checking if you have the product.
We’ve drafted a message you can send Akorn to request your refund or repair — edit it as you like.
Subject: Recall D-0825-2023 — Akorn Akorn Hello, I own a Akorn that is covered by recall D-0825-2023 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.
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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.
