Recall RadarprednisoLONE Acetate Ophthalmic Suspension, USP, 1%, Rx only, Sterile, a) 5 mL (NDC 70748-332-02); b) 10 mL (NDC 70748-332-03), c) 15 mL (70748-332-04), Manufactured by: Lupin Lim…
Presence of Foreign Substance
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- Lupin Pharmaceuticals Inc. — Naples, FL
- Severity
- Class II — moderate
- Reported
- July 8, 2026
- Quantity
- 2,530,182 bottles
- Recall number
- D-0655-2026
- Status
- Ongoing
- Source
- FDA
Where it went
U.S. Nationwide
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