{"url_path":"/fda/drug/recalls/D-0643-2026","section_key":"summary","section_title":"DRUG Recall: CareFusion 213, LLC — BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), packaged as a) 100 x 10.5 mL applicators/case, NDC 54365-400-35, Catalog Number: 930715NS; b) 100 x 10.5 mL applicators/case, Catalog Number bulk 930715NSB, NDC 54365-400-35; STERILE SOLUTION, CAREFUSION 213, LLC, EL PASO, TX 79912, subsidiary of Beckton, Di…","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-0643-2026%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":141,"has_tables":false,"body_markdown":null}