{"url_path":"/fda/drug/recalls/D-0655-2026","section_key":"summary","section_title":"DRUG Recall: Lupin Pharmaceuticals Inc. — 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","topic":"fda","document":{"doc_type":"drug-recall","doc_date":"2026-06-04","source_url":"https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0655-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Lupin Pharmaceuticals Inc."},"word_count":342,"has_tables":false,"body_markdown":null}