{"url_path":"/fda/device/recalls/Z-2141-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-03-24","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2141-2026%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":110,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2141-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class I\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-03-24\n**Report date:** 2026-05-20\n\n## Product\nNamic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer\n\n## Reason\nMedline has identified the presence of particulate within the fluid path of the Manifolds.\n\n## Affected lots\nUDI/DI each 10193489059137, UDI/DI case 30193489059131, Lot Numbers:  89181, 95326, 95254, 102287, 102286, 102706, 105362, 105558, 108608, 112242, 112243, 115437, 118477, 121180, 121645, 122708, 126024, 131603, 136583, 140860, 142371, 146728, 147474, 148571, 152020, 153175, 163216, 175580, 176810, 184394, 191388, 193141.\n\n## Distribution\nUS (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK."}