PRED MILD recalled over undeclared allergens
- Recall date
- May 18, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- AbbVie Inc. recalls PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie c…
- Recall number
- D-0551-2026
- FDA classification
- Class III
- Brand / firm
- AbbVie Inc.
- Sold / distributed
- US Nationwide.
Why it was recalled
Failed Stability Specifications
Class III means the product violates regulations but is not likely to cause harm.
What was 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.
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