{"url_path":"/fda/device/recalls/Z-2764-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — MEDLINE medical procedure convenience kit labeled as:    HIP CDS-LF, Medline kit SKU CDS984556N","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-08","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2764-2026%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":94,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2764-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class I\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-06-08\n**Report date:** 2026-07-29\n\n## Product\nMEDLINE medical procedure convenience kit labeled as:    HIP CDS-LF, Medline kit SKU CDS984556N\n\n## Reason\nThe procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could result in drug ineffectiveness.\n\n## Affected lots\nUDI/DI 10198459266621 (each) 40198459266622 (case), Lot Numbers:  26EDA285, 26DDA718, 26BDB740, 26ADB079, 26ADA161, 25KDB472, 25GDA213.\n\n## Distribution\nUS:  Mo, CO, IL"}