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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
Agency
Firm
AbbVie Inc.
Recall ID
99008
Status
ONGOING

Why it was recalled

Failed Stability Specifications

How to identify it

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.

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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