{"url_path":"/fda/device/recalls/Z-2333-2026","section_key":"summary","section_title":"DEVICE Recall: Avanos Medical, Inc. — Brand Name: CORFLO  Product Name: CORFLO* Safety PEG Kit  Model/Catalog Number: 30-4320","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-30","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2333-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Avanos Medical, Inc."},"word_count":74,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2333-2026\n\n**Recalling firm:** Avanos Medical, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-30\n**Report date:** 2026-06-17\n\n## Product\nBrand Name: CORFLO  Product Name: CORFLO* Safety PEG Kit  Model/Catalog Number: 30-4320\n\n## Reason\nLidocaine hydrochloride injection, the subject of a supplier recall for  quality issues, were included into sterile kits and sets.\n\n## Affected lots\nUDI-DI 10350770007585, Lot Numbers 30365226 and 30382750\n\n## Distribution\nUS Nationwide distribution."}