Waxaa soo dhigay: Northwest Eye gudaha Wararka Luulyo 14, 2026
At Northwest Eye, your health and safety are our highest priorities. We want to make you aware of a voluntary nationwide recall issued by Lupin Pharmaceuticals Inc. for certain lots of Prednisolone Acetate Ophthalmic Suspension USP 1% (eye drops).
The U.S. Food and Drug Administration (FDA) has classified this as a Class II recall due to the potential presence of a foreign substance in the medication. A Class II recall means use of the affected product may cause temporary or medically reversible health effects, and the risk of serious adverse health consequences is considered low.
What Should You Do?
If you are currently using Prednisolone Acetate 1% eye drops, please take the following steps:
- Check the bottle for the NDC number, lot number, iyo expiration date.
- Compare your medication to the recalled products listed below.
- If your bottle matches an affected lot, contact your pharmacy immediately. Your pharmacy can assist with the recall process and arrange for a replacement bottle or a new prescription if needed.
- Continue your treatment only as directed by your pharmacist and your eye care provider.
Affected Products
The recall includes the following products:
- 5 mL bottle: NDC 70748-332-02
- 10 mL bottle: NDC 70748-332-03
- 15 mL bottle: NDC 70748-332-04
The affected lots have expiration dates ranging from July 31, 2026, through March 31, 2028.
Questions?
If you have questions about your medication or your treatment plan, please don’t hesitate to contact Northwest Eye. Our team is here to help ensure you continue your care safely and confidently.
Thank you for trusting Northwest Eye with your vision and eye health.
