Akorn, Inc. recalls Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake
Failed Stability Specification: OOS low viscosity results discovered during retain testing.
Recall notice
Failed Stability Specification: OOS low viscosity results discovered during retain testing.
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Source Page by GovInfoNow · govinfonow.com/recall/40804-akorn-inc-recalls-atropine-sulfate-ophthalmic-1-solution-usp-5ml · Recall date February 21, 2018 · FDA enforcement record: FDA #D-0577-2018
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“Akorn, Inc. recalls Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake.” GovInfoNow, recall dated February 21, 2018. https://govinfonow.com/recall/40804-akorn-inc-recalls-atropine-sulfate-ophthalmic-1-solution-usp-5ml. Based on FDA recall #D-0577-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0577-2018%22&limit=1).
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Subject: Recall D-0577-2018 — Akorn, Inc. Akorn, Inc. recalls Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Steri Hello, I own a Akorn, Inc. recalls Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake that is covered by recall D-0577-2018 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-0577-2018 (February 21, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0577-2018 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.