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Recall Canary
Pred Mild Ophthalmic Suspension
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DRUG RECALLLOW

Pred Mild Ophthalmic Suspension

AbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.

What to do

Contact your healthcare provider or pharmacist if you have questions or concerns about your medication. Do not stop using the product unless advised by a medical professional.

Posted
Updated
Recall No.
D-0551-2026
Agency
Firm
AbbVie Inc.
Recall ID
99008
Status
ONGOING

Why it was recalled

AbbVie is recalling Pred Mild (prednisolone acetate ophthalmic suspension, USP, 0.12%) due to failed stability specifications. The affected product is a 10 mL sterile prescription eye drop.

Is mine affected?

Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.

PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie company, North Chicago, IL 60064, Product of France, NDC 11980-174-10.

Recall #
D-0551-2026

Where it was sold

Distributed nationwide.

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Editorial summary by Recall Canary · last updated 2026-05-28 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification