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We’ve received questions about the recent FDA eye drop recall of certain Prednisolone Acetate Ophthalmic Suspension USP 1% eye drops.
If you are using the post-operative compounded combination eye drops (purple cap) dispensed by the Tower Clock Surgery Center, they are NOT affected by this recall. These drops are made by a different manufacturer and are safe to continue using as directed.
The recall only applies to certain lots of Prednisolone Acetate Ophthalmic Suspension USP 1% manufactured by Lupin Pharmaceuticals.
If you have a bottle of Prednisolone Acetate 1% from a retail pharmacy, check:
- Manufacturer: Lupin Pharmaceuticals
- Bottle size: 5 mL, 10 mL, or 15 mL
- NDC: 70748-332-02, 70748-332-03, or 70748-332-04
- Expiration dates: July 2026 through February 2028
If you believe you have an affected bottle, please contact your pharmacist or our office so we can help determine the best next step.
For the complete list of affected lot numbers, and for additional information, please visit the FDA recall notice.
