{"url_path":"/fda/device/recalls/Z-2492-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — MEDLINE Medical Procedure Kits labeled as:  CATH 22F ROBINSON STRL 5'S PK, Medline Kit Number/SKU DYNJ0040839","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-2492-2026%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":130,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2492-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-04\n**Report date:** 2026-06-24\n\n## Product\nMEDLINE Medical Procedure Kits labeled as:  CATH 22F ROBINSON STRL 5'S PK, Medline Kit Number/SKU DYNJ0040839\n\n## Reason\nDuring an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.\n\n## Affected lots\nUDI/DI 10889942046126 (each), 40889942046127 (case), Lot Numbers:  25JMK709, 25FMJ661, 25CMG042, 24IME549, 24GMD004, 24CMF091, 24CME465, 24BMH490.\n\n## Distribution\nWorldwide distribution - US Nationwide and the countries of AE, BB, BM, BS, CA, CY, GU, NL, PA, QA, SA, VI."}