{"url_path":"/fda/device/recalls/Z-3023-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline convenience kits labeled as:  LTP CDS-LF, Medline kit SKU CDS980375M","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-07-10","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3023-2026%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":90,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-3023-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-07-10\n**Report date:** 2026-09-02\n\n## Product\nMedline convenience kits labeled as:  LTP CDS-LF, Medline kit SKU CDS980375M\n\n## Reason\nKits contain a potentially contaminated component which were recalled by the manufacturer\n\n## Affected lots\nUDI/DI 10198459447327 (each) 40198459447328 (case), kit lot number 25JBE079.\n\n## Distribution\nUS Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI."}