{"url_path":"/fda/device/recalls/Z-2237-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as:  1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A;  2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B;  3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B;  4) SPINAL TRAY, Medline Kit SKU DYNJRA0255B;  5) SPINAL TRAY, Medline Kit SKU DYNJRA0320;  6) SPINAL TRAY…","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-10","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2237-2026%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":4595,"has_tables":false,"body_markdown":null}