AbbVie Inc. recalls PRED MILD
- Recalling company
- AbbVie Inc.
- Product
- 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.
- Reason
- Failed Stability Specifications
- Classification
- Class III – not likely to cause adverse health consequences
- Recall date
- May 18, 2026
- Reported
- Jun 3, 2026
- Distribution
- US Nationwide.
- Status
- Ongoing
- Quantity
- 2,736 bottles
- Lot / codes
- Lot # 402805, 407596, Exp Date: 08/2026.
- Company location
- North Chicago, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0551-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0551-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.