{"url_path":"/fda/device/recalls/Z-2454-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline Convenience Kits:   1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142;   2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-06","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2454-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Medline Industries, LP"},"word_count":118,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2454-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class I\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-06\n**Report date:** 2026-07-01\n\n## Product\nMedline Convenience Kits:   1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142;   2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407\n\n## Reason\nThe Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.\n\n## Affected lots\n1) ACC011142, UDI-DI: 10198459721342(each), 40198459721343(case), Lot Number: 26DDA462; 2) ACC011142, UDI-DI: 10198459721342(each), 40198459721343(case), Lot Number: 26DDA547; 3) DYNJ8407, UDI-DI: 10198459704543(each), 40198459704544(case), Lot Number: 26DBB599\n\n## Distribution\nUS Nationwide."}