{"url_path":"/fda/drug/recalls/D-0647-2026","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) packaged as a) 100 x 3 mL applicators/case, NDC 54365-400-33, calatog 930415NS: b) 250 x 3mL applicators/case, bulk catalog number 930415NSB; STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co.","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-0647-2026%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":184,"has_tables":false,"body_markdown":null}