{"url_path":"/fda/device/recalls/Z-3134-2026","section_key":"summary","section_title":"DEVICE Recall: Nipro Renal Soultions USA, Corporation — MedicaLyte Bicarbonate Powder    REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-08-05","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3134-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Nipro Renal Soultions USA, Corporation"},"word_count":85,"has_tables":false,"body_markdown":null}