{"url_path":"/fda/device/recalls/Z-2447-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline convenience kits:    HYSTERECTOMY PACK-LF  DYNJ20485L","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-27","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2447-2026%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":71,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2447-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-27\n**Report date:** 2026-06-24\n\n## Product\nMedline convenience kits:    HYSTERECTOMY PACK-LF  DYNJ20485L\n\n## Reason\nKits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.\n\n## Affected lots\nUDI-DI 10195327024369 Lot 25LMJ031\n\n## Distribution\nUS Nationwide distribution. OUS distribution pending."}