{"url_path":"/fda/device/recalls/Z-2606-2026","section_key":"summary","section_title":"DEVICE Recall: Medline Industries, LP — Medline Convenience kits containing recalled Swan-Ganz Catheters    RIGHT HEART CATH PACK CTX\t  \tDYNJ68530B","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-28","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2606-2026%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":131,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2606-2026\n\n**Recalling firm:** Medline Industries, LP\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-28\n**Report date:** 2026-07-08\n\n## Product\nMedline Convenience kits containing recalled Swan-Ganz Catheters    RIGHT HEART CATH PACK CTX\t  \tDYNJ68530B\n\n## Reason\nKits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.\n\n## Affected lots\nUDI-DI 10195327345044   Lots  23DBI807  23FBG708  23GBK642  23KBO477  24BBG198  24FBN889  24GBJ879  24HBR045  24LBT492  25ABL957  25BBN572  25GBT734  25HBQ817  25LBM617  26BBK766  26DBE720\n\n## Distribution\nUS Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI."}