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Class III · Lower riskActive recall

Pred Mild

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot # 402805, 407596, Exp Date: 08/2026.
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Failed Stability Specifications

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byAllergan, Inc.
Brand namePRED MILD
Generic namePREDNISOLONE ACETATE
Active ingredient(s)PREDNISOLONE ACETATE
Distributed by / forAbbVie Inc.
NDC11980-174-10
Show the full FDA record
Full product labelPRED 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 firmAbbVie Inc.
DistributionUS Nationwide.
Quantity2,736 bottles
Recall initiated2026-05-18
Report date2026-06-03
Recall completed—
Recall numberD-0551-2026
ClassificationClass III
FDA statusOngoing
Origin on fileNorth Chicago IL United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.