United StatesPRED MILD prednisolone acetate ophthalmic suspension, USP 0.12%, 10 mL (NDC 11980-174-10), Product of France, distributed by AbbVie/Allergen, Lot #402805 and #407596, Exp. 08/2026, is being recalled. AbbVie Inc. initiated the ongoing nationwide U.S. recall because the product failed stability specifications.
What's being 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.
Recalling firm: AbbVie Inc., North Chicago, IL, United States.
How to identify it
Lot # 402805, 407596, Exp Date: 08/2026.
The hazard
Failed Stability Specifications
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)