{"url_path":"/fda/device/recalls/Z-3019-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline convenience kits labeled as:    1) FEMORAL PACK, Medline Kit SKU DYNJ909393A;   2) FEVAR, Medline Kit SKU DYNJ910295D.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-07-10","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3019-2026%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":114,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-3019-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-07-10\n**Report date:** 2026-09-02\n\n## Product\nMedline convenience kits labeled as:    1) FEMORAL PACK, Medline Kit SKU DYNJ909393A;   2) FEVAR, Medline Kit SKU DYNJ910295D.\n\n## Reason\nKits contain a potentially contaminated component which were recalled by the manufacturer\n\n## Affected lots\n1) Medline Kit SKU DYNJ909393A, UDI/DI  10195327613945 (each) 40195327613946 (case) Lot Number 25ILA297;  2) Medline Kit SKU DYNJ910295D, UDI/DI 10198459586477 (each) 40198459586478 (case), Lot Number 26CBT178.\n\n## Distribution\nUS Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD, MO, MS, MT, NV, NY, OH, OK, SC, TX, WI."}