Data Composite

Recall D-0655-2026

US Class II Ongoing · initiated 2026-06-04

Recalling firm

Lupin Pharmaceuticals Inc., FL

Product

prednisoLONE 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 Limited, Pithampur (M.P) 454 775, INDIA

Reason for recall

Presence of Foreign Substance

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