{"url_path":"/fda/drug/recalls/D-0644-2026","section_key":"summary","section_title":"DRUG Recall: CareFusion 213, LLC — BD PurPrep,  (Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w), 50 x 26 mL Applicator/case, STERILE SOLUTION, CAREFUSION 213, LLC, EL PASO, TX 79912, subsidiary of Beckton, Dickson and Co, Catalog Number 960120NSB; NDC 54365-014-42.","topic":"fda","document":{"doc_type":"drug-recall","doc_date":"2026-06-11","source_url":"https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0644-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"CareFusion 213, LLC"},"word_count":107,"has_tables":false,"body_markdown":null}