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FDAClass III

PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx onl… Recalled: Failed Stability Specifications

PRED MILD, prednisolone acetate ophthalmic suspension, USP,… was recalled on May 18, 2026 in cooperation with the U.S. Food and Drug Administration because failed Stability Specifications.

Is my unit affected?

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.

Model, lot & date codes to check

Lot # 402805, 407596, Exp Date: 08/2026.

Units affected: 2,736 bottles

Where it was sold: US Nationwide.

Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.

What's the hazard?

Failed Stability Specifications

Class III means the product is unlikely to cause a health problem, but it violates FDA labeling or manufacturing rules.

Your remedy & how to claim it

Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.

Contact: Recalling firm: AbbVie Inc.

Not sure what you're entitled to? Read our guide: what to do if your product is recalled.

Official recall notice

Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.

View official notice →

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