{"url_path":"/fda/device/recalls/Z-2342-2026","section_key":"summary","section_title":"DEVICE Recall: Avanos Medical, Inc. — Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit  20 Fr  PUSH OTW  Model/Catalog Number: 7170-20  Product Description: Feeding Tube Kit  Component: No","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-2342-2026%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":91,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2342-2026\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\nProduct Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit  20 Fr  PUSH OTW  Model/Catalog Number: 7170-20  Product Description: Feeding Tube Kit  Component: No\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\nLot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746\n\n## Distribution\nUS Nationwide distribution."}