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PRED MILD, prednisolone acetate ophthalmic suspension recall

AbbVie Inc. recalled PRED MILD, prednisolone acetate ophthalmic suspension on June 3, 2026 because of failed stability specifications. It was sold nationwide.

Why it was recalled

Failed Stability Specifications

What's recalled

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.

Quantity: 2,736 bottles

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
AbbVie Inc., North Chicago, IL
Date
Severity
Class III
the product is unlikely to cause health problems but breaks a rule.
Where sold
Nationwide
US Nationwide.
Status
Ongoing
Recall number
D-0551-2026
Source
U.S. Food and Drug Administration

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