AbbVie recalls PRED MILD prednisolone acetate ophthalmic suspension due to failed stability specifications. This medication may degrade over time, potentially affecting safety and effectiveness.
Failed Stability Specifications
AbbVie is recalling PRED MILD ophthalmic suspension because it failed stability tests. This means the medication could become less effective or unsafe over time, especially if stored improperly.
The medication may degrade over time, leading to reduced effectiveness or potential safety issues. This happens because the product did not meet stability requirements during testing.
People prescribed this medication by a doctor who received it between 2023 and 2026 are likely affected. Those with eye conditions requiring long-term use are at higher risk.
Check for the product name 'PRED MILD', strength 0.12%, 10 mL, and the lot numbers 402805 or 407596. It was sold with an expiration date of August 2026.
Look for the lot numbers 402805 or 407596 on the label.
The recall is due to failed stability specifications, which could affect effectiveness or safety over time. Consult your doctor for advice.
Check the lot numbers on the label. If it matches 402805 or 407596, contact your doctor or pharmacist for guidance.
The expiration date is August 2026, but the recall indicates it may not meet stability requirements after that date.
We’ve drafted a message you can send AbbVie to request your refund or repair — edit it as you like.
Subject: Recall D-0551-2026 — AbbVie AbbVie Hello, I own a AbbVie that is covered by recall D-0551-2026 from AbbVie. 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.
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