{"url_path":"/fda/device/recalls/Z-2496-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — MEDLINE Medical Procedure Kits labeled as:    1) CV DRAPING/BASIN, Medline Kit Number/SKU DYNJ908483A;   2) CV DRAPING/BASIN, Medline Kit Number/SKU DYNJ908483B;   3) CV DRAPING/BASIN, Medline Kit Number/SKU DYNJ908483C;   4) CV DRAPING/BASIN 2PART PACK, Medline Kit Number/SKU DYNJ89414;   5) CVG BASIN PACK SC, Medline Kit Number/SKU DYNJ38052G;   6) T/A BA…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-04","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2496-2026%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":881,"has_tables":false,"body_markdown":null}