{"url_path":"/fda/device/recalls/Z-2040-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as:   1. BLOOD CULTURE KIT, Medline Kit SKU DYNDH1520;   2. BLOOD DRAW KIT, Medline Kit SKU EBSI1317.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-16","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2040-2026%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":169,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2040-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-03-16\n**Report date:** 2026-05-06\n\n## Product\nMedline medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as:   1. BLOOD CULTURE KIT, Medline Kit SKU DYNDH1520;   2. BLOOD DRAW KIT, Medline Kit SKU EBSI1317.\n\n## Reason\nMedline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.\n\n## Affected lots\nMedline Kit SKU DYNDH1520:  UDI/DI each 10193489197679, UDI/DI case 20193489197676, Lot Number : 2025101301;  Medline Kit SKU DYNDH1520:  UDI/DI each 10193489197679, UDI/DI case 20193489197676, Lot Number : 2025113001;  Medline Kit SKU EBSI1317:  UDI/DI each 10193489195804, UDI/DI case 20193489195801, Lot Number : 2025120390;  Medline Kit SKU EBSI1317:  UDI/DI each 10193489195804, UDI/DI case 20193489195801, Lot Number : 2026022390.\n\n## Distribution\nUS Nationwide distribution."}